Canonical Allele Identifier: PA2826258730
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Arg580Gln
CA234868
NM_001202435.3:c.1739G>A