Canonical Allele Identifier: PA2741921711
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_005369.2:p.Pro337Thr
CA345932075
NM_005378.6:c.1009C>A