Allele Registry

Canonical Allele Identifier: PA2826561211

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420217

RCV000420881

RCV000423272

RCV000429840

RCV000430889

RCV000433950

RCV000435696

RCV000440493

RCV000441630

RCV000785347

RCV001025280

RCV003509529

ClinVar Variation:

376660

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Ser176Ile	CA16603075 NM_001276696.3:c.527G>T CA3047147247 NM_001276696.3:c.527_528delinsTA