Canonical Allele Identifier: PA2827939397
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 12574
ClinVar RCV Id: RCV000013402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341799.1:p.Pro71Ser
CA122520
NM_001354870.1:c.211C>T