Allele Registry

Canonical Allele Identifier: PA2826559858

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000419208

RCV000420300

RCV000423298

RCV000425130

RCV000428749

RCV000429935

RCV000430980

RCV000437595

RCV000438183

RCV000440629

RCV000444464

RCV000785279

RCV001201781

RCV001559774

RCV002365462

RCV004022256

ClinVar Variation:

376693

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Tyr197Cys	CA16603106 NM_001276695.3:c.590A>G