Canonical Allele Identifier: PA1139743820
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 972435
ClinVar RCV Id: RCV001248466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361665.1:p.Leu7655Pro
CA3866079
NM_001374736.1:c.22964T>C