Canonical Allele Identifier: PA2826177240
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1337015
ClinVar RCV Id: RCV001819501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Val706Phe
CA4342889
NM_001193307.1:c.2116G>T