Canonical Allele Identifier: PA2826177265
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378843
ClinVar RCV Id: RCV001914704 RCV002552783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.His737Arg
CA4342874
NM_001193307.1:c.2210A>G