Canonical Allele Identifier: PA2826831043
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2650695
ClinVar RCV Id: RCV003407166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280160.1:p.Pro126Thr
CA345932075
NM_001293231.2:c.376C>A