Canonical Allele Identifier: PA2827784486
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 662029
ClinVar RCV Id: RCV000819574
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ala214Thr
CA349074256
NM_001353958.2:c.640G>A