Canonical Allele Identifier: PA2826830959
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2788480
ClinVar RCV Id: RCV003674087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280157.1:p.Asp265Gly
CA1538245
NM_001293228.1:c.794A>G