Allele Registry

Canonical Allele Identifier: PA168659

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000131726

RCV000475086

RCV000785479

RCV001310211

RCV001781474

RCV003467184

ClinVar Variation:

142536

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119587.1:p.Arg205Cys	CA000010 NM_001126115.1:c.613C>T