Canonical Allele Identifier: PA1139743831
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_001361665.1:p.Asp7813Asn
CA139162135
NM_001374736.1:c.23437G>A