Canonical Allele Identifier: PA2828180367
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1469489
ClinVar RCV Id: RCV001993915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu421Ile
CA349085759
NM_001365536.1:c.1261T>A