Canonical Allele Identifier: PA2829064481
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 357619
ClinVar RCV Id: RCV000382365 RCV000522851 RCV001086062 RCV002411249 RCV003950270
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373029.1:p.Arg470His
CA3871493
NM_001386100.1:c.1409G>A