Canonical Allele Identifier: PA2827784442
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 958506
ClinVar RCV Id: RCV001231687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Thr184Ile
CA349075445
NM_001353958.2:c.551C>T