Allele Registry

Canonical Allele Identifier: PA2828541052

Gene: DST HGNC NCBI

ClinVar RCV:

RCV000382365

RCV000522851

RCV001086062

RCV002411249

RCV003950270

ClinVar Variation:

357619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361658.1:p.Arg470His	CA3871493 NM_001374729.1:c.1409G>A