Allele Registry

Canonical Allele Identifier: PA2741872545

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV003792645

ClinVar Variation:

2931623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile731Thr	CA349079761 NM_001365536.1:c.2192T>C