Allele Registry

Canonical Allele Identifier: PA916045336

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000476670

RCV001131847

RCV001131848

RCV001131849

RCV002323791

RCV003332181

ClinVar Variation:

415031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Lys1056Arg	CA1944130 NM_001365536.1:c.3167A>G