Canonical Allele Identifier: PA2826013128
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1385928
ClinVar RCV Id: RCV001889064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Leu1290Val
CA349053111
NM_001165964.3:c.3868C>G