Canonical Allele Identifier: PA122527
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 12577
ClinVar RCV Id: RCV000013405 RCV003159073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002458.2:p.Pro74Ala
CA122526
NM_002467.6:c.220C>G