Allele Registry

Canonical Allele Identifier: PA2828180700

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001921372

ClinVar Variation:

1424057

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Arg1007Gly	CA1944154 NM_001365536.1:c.3019C>G