Canonical Allele Identifier: PA2826010075
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1405896
ClinVar RCV Id: RCV001915567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ile1224Val
CA349055844
NM_001165963.4:c.3670A>G