Canonical Allele Identifier: PA2741872596
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2946073
ClinVar RCV Id: RCV003806359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile990Asn
CA349074653
NM_001365536.1:c.2969T>A