Canonical Allele Identifier: PA2827789374
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ile1516Val
CA284976
NM_001353960.2:c.4546A>G