Canonical Allele Identifier: PA2826831065
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 13892
ClinVar RCV Id: RCV000014906 RCV001564807 RCV001849263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280160.1:p.Arg182His
CA257009
NM_001293231.2:c.545G>A