Canonical Allele Identifier: PA645405063
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 373157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Gly1749Arg
CA16042389
NM_001165963.4:c.5245G>A
CA349068398
NM_001165963.4:c.5245G>C