Canonical Allele Identifier: PA2829832723
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 1054875
ClinVar RCV Id: RCV001363464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056363.2:p.Leu5008Phe
CA139164585
NM_015548.5:c.15022C>T