Canonical Allele Identifier: PA645407629
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 376300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002458.2:p.Thr73Ile
CA16602746
NM_002467.6:c.218C>T