Allele Registry

Canonical Allele Identifier: PA2826562455

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000685555

ClinVar Variation:

565884

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Val113Ala	CA397836997 NM_001276697.3:c.338T>C