Allele Registry

Canonical Allele Identifier: PA2829832707

Gene: DST HGNC NCBI

ClinVar RCV:

RCV001239513

RCV002402756

ClinVar Variation:

965145

HGVS (amino-acid)	Matching Registered Transcripts
NP_056363.2:p.Asn4982Ser	CA364504860 NM_015548.5:c.14945A>G