Canonical Allele Identifier: PA2827772567
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2711932
ClinVar RCV Id: RCV003590512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Arg222Gly
CA349074150
NM_001353952.2:c.664C>G