Allele Registry

Canonical Allele Identifier: PA2825609627

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001327661

ClinVar Variation:

1027110

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119587.1:p.Leu13Arg	CA397842416 NM_001126115.1:c.38T>G CA645589119 NM_001126115.1:c.38_39delinsGT