Canonical Allele Identifier: PA2827780472
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ile1533Val
CA284976
NM_001353955.2:c.4597A>G