Allele Registry

Canonical Allele Identifier: PA2826566787

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000165724

RCV000804037

RCV000986051

RCV001192618

ClinVar Variation:

186179

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Thr116Ser	CA000210 NM_001276761.3:c.347C>G CA397842094 NM_001276761.3:c.346A>T