Canonical Allele Identifier: PA2827776944
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Gly1221Arg
CA284928
NM_001353954.2:c.3661G>C