Canonical Allele Identifier: PA2827749569
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 453000
ClinVar RCV Id: RCV000524084 RCV001070318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Arg187Trp
CA349075415
NM_001353948.2:c.559C>T