Canonical Allele Identifier: PA2827772365
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ile91Thr
CA285081
NM_001353952.2:c.272T>C