Canonical Allele Identifier: PA2827772536
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2099984
ClinVar RCV Id: RCV003014183
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Tyr202Cys
CA349074429
NM_001353952.2:c.605A>G