Canonical Allele Identifier: PA2827788282
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1474345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ile810Thr
CA349062561
NM_001353960.2:c.2429T>C