Canonical Allele Identifier: PA2579936039
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376679
ClinVar RCV Id: RCV000421406 RCV000422095 RCV000424159 RCV000427021 RCV000426404 RCV000428833 RCV000431660 RCV000434430 RCV000437297 RCV000439053 RCV000439742 RCV000443298 RCV000443877 RCV000444003 RCV000633347 RCV002338982 RCV004022250
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Tyr163Asn
CA16603093
NM_000546.6:c.487T>A