Canonical Allele Identifier: PA2827789550
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ile1627Met
CA256596
NM_001353960.2:c.4881C>G