Canonical Allele Identifier: PA2499253495
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1192891
ClinVar RCV Id: RCV001555098
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val947Ala
CA349076986
NM_001365536.1:c.2840T>C