Canonical Allele Identifier: PA2827788982
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2026678
ClinVar RCV Id: RCV002889282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ser1299Ala
CA349052943
NM_001353960.2:c.3895T>G