Canonical Allele Identifier: PA285152
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Leu1276Pro
CA285150
NM_006920.6:c.3827T>C