Canonical Allele Identifier: PA2826009219
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2848903
ClinVar RCV Id: RCV003754688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Arg393Gly
CA349071039
NM_001165963.4:c.1177C>G