Allele Registry

Canonical Allele Identifier: PA2825868717

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001239513

RCV002402756

ClinVar Variation:

965145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138242.1:p.Asn5348Ser	CA364504860 NM_001144770.2:c.16043A>G