Canonical Allele Identifier: PA2826177242
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2796150
ClinVar RCV Id: RCV003668026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Lys707Thr
CA368193016
NM_001193307.1:c.2120A>C