Allele Registry

Canonical Allele Identifier: PA916010791

Gene: SCN11A HGNC NCBI

ClinVar RCV:

RCV000795168

RCV002345751

ClinVar Variation:

641838

HGVS (amino-acid)	Matching Registered Transcripts
NP_054858.2:p.Gly1695Asp	CA2321402 NM_014139.3:c.5084G>A