Allele Registry

Canonical Allele Identifier: PA2826560469

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 480745

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Met27Ile	CA397846006 NM_001276696.3:c.81G>A CA397846013 NM_001276696.3:c.81G>T CA397846016 NM_001276696.3:c.81G>C