Allele Registry

Canonical Allele Identifier: PA2826561791

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000776836

ClinVar Variation:

630832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Asp285Tyr	CA397835843 NM_001276696.3:c.853G>T