Canonical Allele Identifier: PA2499251651
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1210876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Lys2007Glu
CA59797669
NM_001353948.2:c.6019A>G