Canonical Allele Identifier: PA2827786387
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1382067
ClinVar RCV Id: RCV001922132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Gly1504Arg
CA349072354
NM_001353958.2:c.4510G>A
CA349072356
NM_001353958.2:c.4510G>C