Allele Registry

Canonical Allele Identifier: PA2827939397

Gene: MYC HGNC NCBI

ClinVar RCV:

RCV000013402

ClinVar Variation:

12574

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341799.1:p.Pro71Ser	CA122520 NM_001354870.1:c.211C>T