Canonical Allele Identifier: PA645407630
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 376458
ClinVar RCV Id: RCV000420006 RCV000426528 RCV000437207 RCV000438328 RCV000445053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002458.2:p.Thr73Pro
CA4875250
NM_002467.6:c.217A>C