Allele Registry

Canonical Allele Identifier: PA658681786

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV001888788

ClinVar Variation:

1385370

HGVS (amino-acid)	Matching Registered Transcripts
NP_002968.1:p.Arg1150Gln	CA1944039 NM_002977.3:c.3449G>A