Original source

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

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

Chromosome 15:44574997 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 22 transcripts.

Variant displays