Allele Registry

Canonical Allele Identifier: PA2579936038

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.6708604299

Score -0.072442842

Score 1.2860517474

Score -0.7151991708

Linked Data - NCBI & NCI

ClinVar Allele:

363559

ClinVar RCV:

RCV000417511

RCV000418221

RCV000418859

RCV000423239

RCV000423893

RCV000425645

RCV000428451

RCV000431265

RCV000434193

RCV000435900

RCV000436639

RCV000438678

RCV000440924

RCV000441609

RCV001023195

RCV001071488

RCV002289543

RCV003476012

ClinVar Variation:

376680

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr163His	CA16603094 NM_000546.6:c.487T>C