Allele Registry

Canonical Allele Identifier: PA2826561069

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001201971

ClinVar Variation:

933702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Leu149Val	CA397840905 NM_001276696.3:c.445C>G