Canonical Allele Identifier: PA2827760093
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1455814
ClinVar RCV Id: RCV001946710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Asp1405Gly
CA349049938
NM_001353949.2:c.4214A>G