Allele Registry

Canonical Allele Identifier: PA916006493

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 186132

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Thr63Ile	CA000098 NM_001276761.3:c.188C>T