Canonical Allele Identifier: PA2827773567
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68602
ClinVar RCV Id: RCV000059479 RCV000636356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Val933Ala
CA285093
NM_001353952.2:c.2798T>C