Canonical Allele Identifier: PA2827772565
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Leu221Pro
CA317148
NM_001353952.2:c.662T>C