Canonical Allele Identifier: PA2825868785
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 1051434
ClinVar RCV Id: RCV002548536 RCV001359472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138242.1:p.Val5490Met
CA3865990
NM_001144770.2:c.16468G>A