Allele Registry

Canonical Allele Identifier: PA2499244547

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001302774

ClinVar Variation:

1005829

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Leu98Val	CA397842729 NM_001276761.3:c.292C>G