Canonical Allele Identifier: PA191098
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro72His
CA000071
NM_001126114.3:c.215C>A