Canonical Allele Identifier: PA2827939393
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 12576
ClinVar RCV Id: RCV000013404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341799.1:p.Glu53Asp
CA122524
NM_001354870.1:c.159G>C
CA372279483
NM_001354870.1:c.159G>T