Canonical Allele Identifier: PA645407626
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 376459
ClinVar RCV Id: RCV000418915 RCV000427867 RCV000428982 RCV000436178 RCV000438593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002458.2:p.Pro58Leu
CA16602893
NM_002467.6:c.173C>T