Canonical Allele Identifier: PA2827772202
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ile1944Met
CA317108
NM_001353951.2:c.5832A>G