Canonical Allele Identifier: PA285128
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Thr112Ile
CA285126
NM_006920.6:c.335C>T