Canonical Allele Identifier: PA2826260195
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Cys1588Arg
CA284979
NM_001202435.3:c.4762T>C