Canonical Allele Identifier: PA2828545959
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_001361663.1:p.Leu7640Phe
CA139164585
NM_001374734.1:c.22918C>T