Allele Registry

Canonical Allele Identifier: PA916045369

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001513087

RCV001726204

RCV001807278

RCV001807279

RCV001807280

RCV001811006

ClinVar Variation:

440255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Trp1161Arg	CA1944040 NM_001365536.1:c.3481T>C CA349070804 NM_001365536.1:c.3481T>A