Canonical Allele Identifier: PA2827788919
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Leu1258Pro
CA285150
NM_001353960.2:c.3773T>C