Canonical Allele Identifier: PA2826259256
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Cys959Arg
CA285105
NM_001202435.3:c.2875T>C