Canonical Allele Identifier: PA2829604436
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2105662
ClinVar RCV Id: RCV003014978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005369.2:p.Asp265Val
CA345931615
NM_005378.6:c.794A>T