Canonical Allele Identifier: PA2827779843
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1335962
ClinVar RCV Id: RCV001822144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Cys1168Arg
CA349056592
NM_001353955.2:c.3502T>C