Allele Registry

Canonical Allele Identifier: PA106893

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376575

ClinVar RCV Id: RCV000418923 RCV000419485 RCV000423226 RCV000424531 RCV000425465 RCV000425867 RCV000424302 RCV000429749 RCV000432222 RCV000434344 RCV000435732 RCV000434584 RCV000440842 RCV000439773 RCV000441115 RCV000442527 RCV000442617 RCV001067780 RCV001523834 RCV001551247 RCV002289520

ClinVar Variation Id: 485039

ClinVar RCV Id: RCV000565464 RCV003509567

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys238Ser	CA16603001 NM_000546.6:c.713G>C CA397839198 NM_000546.6:c.712T>A