Canonical Allele Identifier: PA2826561079
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 418517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro151Leu
CA16620625
NM_001276696.3:c.452C>T