Allele Registry

Canonical Allele Identifier: PA2826560328

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003464701

ClinVar Variation:

2679234

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Leu284Val	CA397835860 NM_001276695.3:c.850C>G