Canonical Allele Identifier: PA2829066190
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 1054875
ClinVar RCV Id: RCV001363464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373029.1:p.Leu5328Phe
CA139164585
NM_001386100.1:c.15982C>T