Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 4:155506947 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940775

Most severe consequence
Clinical significance

Synonyms

LSDB 1935

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

4:g.155506947T>A
ENST00000302053.3:c.1634A>T
ENSP00000306361.3:p.Glu545Val
ENST00000403106.3:c.1634A>T
ENSP00000385981.3:p.Glu545Val

Variation displays