Allele Registry

Canonical Allele Identifier: PA2829066208

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001510452

RCV001664906

RCV001664907

ClinVar Variation:

1164480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373029.1:p.Ala5362Thr	CA3866054 NM_001386100.1:c.16084G>A