Allele Registry

Canonical Allele Identifier: PA2579936299

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001327661

ClinVar Variation:

1027110

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Leu145Arg	CA397842416 NM_000546.6:c.434T>G CA645589119 NM_000546.6:c.434_435delinsGT