Canonical Allele Identifier: PA2827769064
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 567303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ala104Asp
CA349077094
NM_001353951.2:c.311C>A