Canonical Allele Identifier: PA2827778437
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2742755
ClinVar RCV Id: RCV003589215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Pro151His
CA349075898
NM_001353955.2:c.452C>A