Canonical Allele Identifier: PA2826259954
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ala1441Pro
CA284958
NM_001202435.3:c.4321G>C