Allele Registry

Canonical Allele Identifier: PA1139742831

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001208223

RCV001528173

ClinVar Variation:

938920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Arg907Gln	CA59794605 NM_001365536.1:c.2720G>A