Canonical Allele Identifier: PA2827781269
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2040195
ClinVar RCV Id: RCV002886300 RCV004066013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Asn47Ser
CA349243068
NM_001353957.2:c.140A>G