Canonical Allele Identifier: PA916036662
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68619
ClinVar RCV Id: RCV000059496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ser417Arg
CA285135
NM_001353961.2:c.1251T>A
CA349055681
NM_001353961.2:c.1251T>G
CA349055688
NM_001353961.2:c.1249A>C