Canonical Allele Identifier: PA2827774074
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Leu1298Phe
CA266111
NM_001353952.2:c.3892C>T