Allele Registry

Canonical Allele Identifier: PA2828179937

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006742

RCV000302710

RCV000309032

RCV000402111

RCV000532835

ClinVar Variation:

6370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Gln10Arg	CA253850 NM_001365536.1:c.29A>G