Allele Registry

Canonical Allele Identifier: PA2828180413

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001319113

ClinVar Variation:

1019651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ser459Leu	CA1944517 NM_001365536.1:c.1376C>T