Canonical Allele Identifier: PA2573205627
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1382067
ClinVar RCV Id: RCV001922132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Gly718Arg
CA349072354
NM_001353961.2:c.2152G>A
CA349072356
NM_001353961.2:c.2152G>C