Allele Registry

Canonical Allele Identifier: PA145436

Gene: SCN11A HGNC NCBI

ClinVar RCV:

RCV000074496

ClinVar Variation:

89013

HGVS (amino-acid)	Matching Registered Transcripts
NP_054858.2:p.Ala808Gly	CA145435 NM_014139.3:c.2423C>G