Canonical Allele Identifier: PA122292
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Pro19Thr
CA000198
NM_001126116.1:c.55C>A