Canonical Allele Identifier: PA108264
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68619
ClinVar RCV Id: RCV000059496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ser1231Arg
CA285135
NM_001165963.4:c.3693T>A
CA349055681
NM_001165963.4:c.3693T>G
CA349055688
NM_001165963.4:c.3691A>C