Canonical Allele Identifier: PA2826013356
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1739737
ClinVar RCV Id: RCV002332074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp1415His
CA349049553
NM_001165964.3:c.4243G>C