Canonical Allele Identifier: PA2827754044
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ile1545Val
CA284976
NM_001353948.2:c.4633A>G