Canonical Allele Identifier: PA2827771303
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1403815
ClinVar RCV Id: RCV001901322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ala1418Val
CA349049642
NM_001353951.2:c.4253C>T