Canonical Allele Identifier: PA2826011439
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 567303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ala104Asp
CA349077094
NM_001165964.3:c.311C>A