Allele Registry

Canonical Allele Identifier: PA2579935195

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.022484333

Score 0.7644029201

Score 0.03175217

Score 0.286749714

Score 0.402566612

Score -0.9051926432

Score 0.790009905

Score -0.066628829

Score 1.6164112665

Score -0.024725173

Score 0.482060663

Score -0.470878468

Score 0.759675159

Score -0.170739614

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000223044

RCV000421256

RCV000423612

RCV000424282

RCV000426851

RCV000428477

RCV000432300

RCV000433419

RCV000434302

RCV000439114

RCV000441535

RCV000442741

RCV000560536

RCV001355898

RCV003137828

RCV003475037

RCV004020697

ClinVar Variation:

234036

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asn239Asp	CA10580926 NM_000546.6:c.715A>G