Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:17387331 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043296

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9660, 2010_April_001_203_KCNJ11_600937_0011

This variation has 5 HGVS names - click the plus to show

11:g.17387331G>A
ENST00000528731.1:c.500C>T
ENSP00000434755.1:p.Pro167Leu
ENST00000339994.4:c.761C>T
ENSP00000345708.4:p.Pro254Leu

Variation displays