Allele Registry

Canonical Allele Identifier: PA645432597

Gene: SCN11A HGNC NCBI

ClinVar RCV:

RCV000488990

RCV000489242

ClinVar Variation:

426113

HGVS (amino-acid)	Matching Registered Transcripts
NP_054858.2:p.Leu396Pro	CA352168024 NM_014139.3:c.1187T>C