Canonical Allele Identifier: PA2828474058
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2939721
ClinVar RCV Id: RCV003794887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asn298Ser
CA59728758
NM_001371247.1:c.893A>G