Canonical Allele Identifier: PA2827749616
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2099984
ClinVar RCV Id: RCV003014183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Tyr202Cys
CA349074429
NM_001353948.2:c.605A>G