Canonical Allele Identifier: PA2829676453
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 373157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly1738Arg
CA16042389
NM_006920.6:c.5212G>A
CA349068398
NM_006920.6:c.5212G>C