Canonical Allele Identifier: PA302803
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 195131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.His127Asp
CA302801
NM_001165963.4:c.379C>G