Canonical Allele Identifier: PA2827779378
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1474345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ile827Thr
CA349062561
NM_001353955.2:c.2480T>C