Canonical Allele Identifier: PA2826177270
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050603
ClinVar RCV Id: RCV001358236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Thr745Ala
CA368192016
NM_001193307.1:c.2233A>G