Canonical Allele Identifier: PA2827790116
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1210876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Lys1978Glu
CA59797669
NM_001353960.2:c.5932A>G