Original source

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

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

Chromosome 4:155506864 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930251

Most severe consequence
Clinical significance

Synonyms

LSDB 1936

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

4:g.155506864G>A
ENST00000302053.3:c.1717C>T
ENSP00000306361.3:p.Arg573Cys
ENST00000403106.3:c.1717C>T
ENSP00000385981.3:p.Arg573Cys

Variation displays