Canonical Allele Identifier: PA2827755013
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Met1780Thr
CA285018
NM_001353948.2:c.5339T>C