Canonical Allele Identifier: PA2827770944
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2313708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Thr1211Ile
CA349055889
NM_001353951.2:c.3632C>T