Canonical Allele Identifier: PA2827784478
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 431844
ClinVar RCV Id: RCV000498818 RCV001857000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Asn211Ser
CA349074293
NM_001353958.2:c.632A>G