Canonical Allele Identifier: PA2826177209
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 985501
ClinVar RCV Id: RCV001266437
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Asn658Asp
CA368193886
NM_001193307.1:c.1972A>G