Canonical Allele Identifier: PA2580222287
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1717244
ClinVar RCV Id: RCV002297464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Phe1359Ser
CA349063759
NM_001365536.1:c.4076T>C