Canonical Allele Identifier: PA2827774499
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ile1534Val
CA284976
NM_001353952.2:c.4600A>G