Allele Registry

Canonical Allele Identifier: PA2825605362

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 647256

ClinVar RCV Id: RCV000801729

ClinVar Variation Id: 2113149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119585.1:p.Ser269Arg	CA397837062 NM_001126113.3:c.807C>G CA397837064 NM_001126113.3:c.807C>A CA397837083 NM_001126113.3:c.805A>C