Allele Registry

Canonical Allele Identifier: PA2826564270

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 647256

ClinVar RCV Id: RCV000801729

ClinVar Variation Id: 2113149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263628.1:p.Ser110Arg	CA397837062 NM_001276699.3:c.330C>G CA397837064 NM_001276699.3:c.330C>A CA397837083 NM_001276699.3:c.328A>C