Allele Registry

Canonical Allele Identifier: PA2826561075

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003064392

ClinVar Variation:

2137906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Ala150Asp	CA397840870 NM_001276696.3:c.449C>A