Allele Registry

Canonical Allele Identifier: PA645407632

Gene: MYC HGNC NCBI

ClinVar RCV:

RCV000424357

ClinVar Variation:

376301

HGVS (amino-acid)	Matching Registered Transcripts
NP_002458.2:p.Ser77Phe	CA16602747 NM_002467.6:c.230C>T