Canonical Allele Identifier: PA2827770205
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1062173
ClinVar RCV Id: RCV001371859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Pro657Thr
CA1943225
NM_001353951.2:c.1969C>A