Canonical Allele Identifier: PA119188
Gene: SMN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059107.1:p.Gly287Arg
CA119187
NM_017411.4:c.859G>C
CA360087005
NM_017411.4:c.859G>A