Canonical Allele Identifier: PA145255
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg1625Gln
CA145253
NM_006920.6:c.4874G>A