Canonical Allele Identifier: PA2827776033
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Arg534His
CA317245
NM_001353954.2:c.1601G>A