Allele Registry

Canonical Allele Identifier: PA2828180107

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006741

ClinVar Variation:

6369

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Pro149Gln	CA118173 NM_001365536.1:c.446C>A