Canonical Allele Identifier: PA2828542999
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 965145
ClinVar RCV Id: RCV001239513 RCV002402756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361658.1:p.Asn7309Ser
CA364504860
NM_001374729.1:c.21926A>G