Canonical Allele Identifier: PA2829675959
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1455814
ClinVar RCV Id: RCV001946710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asp1405Gly
CA349049938
NM_006920.6:c.4214A>G