Canonical Allele Identifier: PA2827778010
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1436471
ClinVar RCV Id: RCV002002115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Leu1829Pro
CA349065632
NM_001353954.2:c.5486T>C