Allele Registry

Canonical Allele Identifier: PA2825866656

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001510452

RCV001664906

RCV001664907

ClinVar Variation:

1164480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138241.1:p.Ala5546Thr	CA3866054 NM_001144769.5:c.16636G>A