Canonical Allele Identifier: PA2827776148
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 588285
ClinVar RCV Id: RCV002314381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ser625Cys
CA349067383
NM_001353954.2:c.1873A>T