Allele Registry

Canonical Allele Identifier: PA916045296

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000020512

ClinVar Variation:

21345

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Leu834Arg	CA341933 NM_001365536.1:c.2501T>G