Canonical Allele Identifier: PA2827939396
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 376299
ClinVar RCV Id: RCV000440255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341799.1:p.Ala58Val
CA4875243
NM_001354870.1:c.173C>T