Canonical Allele Identifier: PA2826258432
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 929416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ala354Pro
CA349071368
NM_001202435.3:c.1060G>C