Canonical Allele Identifier: PA2828546031
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 971778
ClinVar RCV Id: RCV001247638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361663.1:p.Asp7798Asn
CA139162135
NM_001374734.1:c.23392G>A