Allele Registry

Canonical Allele Identifier: PA2828180691

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001338561

ClinVar Variation:

1035664

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Val1002Met	CA349074508 NM_001365536.1:c.3004G>A