Canonical Allele Identifier: PA2827777252
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1455814
ClinVar RCV Id: RCV001946710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Asp1404Gly
CA349049938
NM_001353954.2:c.4211A>G