Canonical Allele Identifier: PA2826012578
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Arg903His
CA303154
NM_001165964.3:c.2708G>A