Canonical Allele Identifier: PA2827757170
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 372865
ClinVar RCV Id: RCV000413776 RCV001328664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Val421Met
CA16042397
NM_001353949.2:c.1261G>A