Canonical Allele Identifier: PA2827785971
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Thr1272Ile
CA317408
NM_001353958.2:c.3815C>T