Allele Registry

Canonical Allele Identifier: PA2826561071

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001881135

ClinVar Variation:

1378428

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Ala150Gly	CA397840857 NM_001276696.3:c.449C>G