Canonical Allele Identifier: PA2826012415
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Thr784Arg
CA284895
NM_001165964.3:c.2351C>G