Canonical Allele Identifier: PA2827789427
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Gly1557Glu
CA285180
NM_001353960.2:c.4670G>A