Allele Registry

Canonical Allele Identifier: PA2827475943

Gene: SCN11A HGNC NCBI

ClinVar RCV:

RCV000074494

ClinVar Variation:

89011

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336182.1:p.Leu811Pro	CA145432 NM_001349253.2:c.2432T>C