Canonical Allele Identifier: PA2826010359
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2833642
ClinVar RCV Id: RCV003754473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Gly1419Arg
CA349049919
NM_001165963.4:c.4255G>C
CA349049920
NM_001165963.4:c.4255G>A