Allele Registry

Canonical Allele Identifier: PA2828180201

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006723

ClinVar Variation:

6351

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ser241Thr	CA340548 NM_001365536.1:c.721T>A