Canonical Allele Identifier: PA2827785961
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2104158
ClinVar RCV Id: RCV003031242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ser1267Pro
CA349053536
NM_001353958.2:c.3799T>C