Canonical Allele Identifier: PA2827777603
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Val1618Met
CA284988
NM_001353954.2:c.4852G>A