Canonical Allele Identifier: PA2827782405
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Thr847Met
CA256587
NM_001353957.2:c.2540C>T