Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A/C|Ancestral: T|Ambiguity code: H
Location

Chromosome 7:2554374 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_031202

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 26 transcripts and has 2 sample genotypes.

Variant displays