Allele Registry

Canonical Allele Identifier: PA2826565401

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000418563

RCV000421434

RCV000422732

RCV000424249

RCV000424653

RCV000429475

RCV000429952

RCV000430137

RCV000432087

RCV000434070

RCV000439276

RCV000440822

RCV000441518

RCV000442369

RCV000445065

RCV000530055

RCV000567103

RCV000785243

RCV003401413

RCV004022205

ClinVar Variation:

376572

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263689.1:p.Cys137Trp	CA16602998 NM_001276760.3:c.411C>G