Canonical Allele Identifier: PA2826012500
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Thr847Met
CA256587
NM_001165964.3:c.2540C>T