Canonical Allele Identifier: PA2828540924
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_001361651.1:p.Val7662Met
CA3866057
NM_001374722.1:c.22984G>A