Allele Registry

Canonical Allele Identifier: PA2825598493

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000587100

RCV000633332

RCV001016637

RCV001016639

RCV002289886

RCV002290531

ClinVar Variation:

496047

528238

821828

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119584.1:p.Ser9Arg	CA003949 NM_001126112.3:c.27C>G CA397849245 NM_001126112.3:c.27C>A CA397849282 NM_001126112.3:c.25A>C