Canonical Allele Identifier: PA2827776596
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Cys947Arg
CA285105
NM_001353954.2:c.2839T>C