Canonical Allele Identifier: PA2827787098
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ile1927Met
CA317108
NM_001353958.2:c.5781A>G