Canonical Allele Identifier: PA916036415
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Thr875Met
CA256587
NM_001353948.2:c.2624C>T