Allele Registry

Canonical Allele Identifier: PA645407627

Gene: MYC HGNC NCBI

ClinVar RCV:

RCV000440255

ClinVar Variation:

376299

HGVS (amino-acid)	Matching Registered Transcripts
NP_002458.2:p.Ala59Val	CA4875243 NM_002467.6:c.176C>T