Canonical Allele Identifier: PA2827939395
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 376459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341799.1:p.Pro57Leu
CA16602893
NM_001354870.1:c.170C>T