Canonical Allele Identifier: PA2828540907
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 1054875
ClinVar RCV Id: RCV001363464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361651.1:p.Leu7631Phe
CA139164585
NM_001374722.1:c.22891C>T