Canonical Allele Identifier: PA2828545977
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 648459
ClinVar RCV Id: RCV000803193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361663.1:p.Val7671Met
CA3866057
NM_001374734.1:c.23011G>A