Allele Registry

Canonical Allele Identifier: PA145433

Gene: SCN11A HGNC NCBI

ClinVar RCV:

RCV000074494

ClinVar Variation:

89011

HGVS (amino-acid)	Matching Registered Transcripts
NP_054858.2:p.Leu811Pro	CA145432 NM_014139.3:c.2432T>C