Canonical Allele Identifier: PA2828541052
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 357619
ClinVar RCV Id: RCV000382365 RCV000522851 RCV001086062 RCV002411249 RCV003950270
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Amino-acid Alleles

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