Canonical Allele Identifier: PA2827752650
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1308538
ClinVar RCV Id: RCV001763450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Arg1213Gly
CA349056062
NM_001353948.2:c.3637C>G