Canonical Allele Identifier: PA2579935334
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376670
ClinVar RCV Id: RCV000417716 RCV000420083 RCV000422099 RCV000427972 RCV000426649 RCV000428855 RCV000431215 RCV000437749 RCV000439081 RCV000437980 RCV000442710 RCV000785309 RCV001042741 RCV002365461 RCV003321589 RCV004022246
ClinVar Variation Id: 406596
ClinVar RCV Id: RCV000466409 RCV001270272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val216Leu
CA16603084
NM_000546.6:c.646G>T
CA16615950
NM_000546.6:c.646G>C