Canonical Allele Identifier: PA2573268195
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060124.2:p.Lys688Arg
CA368193446
NM_017654.4:c.2063A>G