Allele Registry

Canonical Allele Identifier: PA338194

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.9599340903

Score 1.5981325008

Score -1.0923082496

Score 0.410418259

Linked Data - NCBI & NCI

ClinVar Allele:

213398

ClinVar RCV:

RCV000198789

RCV000418938

RCV000419621

RCV000421097

RCV000421751

RCV000423911

RCV000428484

RCV000429211

RCV000429852

RCV000434089

RCV000434805

RCV000436603

RCV000437301

RCV000438726

RCV000439388

RCV000441624

RCV000442071

RCV000487386

RCV000785324

RCV001024600

RCV001271054

RCV002288812

RCV003474953

ClinVar Variation:

216077

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ile195Thr	CA002232 NM_000546.6:c.584T>C