Canonical Allele Identifier: PA2827939398
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 376458
ClinVar RCV Id: RCV000420006 RCV000426528 RCV000437207 RCV000438328 RCV000445053
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341799.1:p.Thr72Pro
CA4875250
NM_001354870.1:c.214A>C