Canonical Allele Identifier: PA2580222242
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2186484
ClinVar RCV Id: RCV002606676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met950Thr
CA349076914
NM_001365536.1:c.2849T>C