Canonical Allele Identifier: PA2827777468
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1382067
ClinVar RCV Id: RCV001922132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Gly1520Arg
CA349072354
NM_001353954.2:c.4558G>A
CA349072356
NM_001353954.2:c.4558G>C