Canonical Allele Identifier: PA916045322
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 538441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Thr977Arg
CA349074841
NM_001365536.1:c.2930C>G