Allele Registry

Canonical Allele Identifier: PA2825616387

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003464701

ClinVar Variation:

2679234

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119589.1:p.Leu191Val	CA397835860 NM_001126117.1:c.571C>G