Canonical Allele Identifier: PA2827770161
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1480447
ClinVar RCV Id: RCV001985935 RCV003120792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Arg617Gly
CA349067458
NM_001353951.2:c.1849A>G