Canonical Allele Identifier: PA2826177207
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1928328
ClinVar RCV Id: RCV002614478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Ile654Asn
CA368193945
NM_001193307.1:c.1961T>A