Allele Registry

Canonical Allele Identifier: PA2826567680

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 492627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Pro279Leu	CA397835952 NM_001276761.3:c.836C>T