Allele Registry

Canonical Allele Identifier: PA2828180108

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001945829

ClinVar Variation:

1427115

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Pro149Leu	CA1944791 NM_001365536.1:c.446C>T