Allele Registry

Canonical Allele Identifier: PA916045403

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000194859

RCV000551270

ClinVar Variation:

212137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Lys1383Arg	CA209307 NM_001365536.1:c.4148A>G