Canonical Allele Identifier: PA2828180374
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 415032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met426Lys
CA1944559
NM_001365536.1:c.1277T>A