Canonical Allele Identifier: PA2499253512
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1026330
ClinVar RCV Id: RCV001326763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Phe1371Ser
CA349063539
NM_001365536.1:c.4112T>C