Canonical Allele Identifier: PA1139736847
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_060124.2:p.Asn658Asp
CA368193886
NM_017654.4:c.1972A>G