Canonical Allele Identifier: PA2826561428
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 420136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro211Leu
CA16620620
NM_001276696.3:c.632C>T
CA645588533
NM_001276696.3:c.632_633delinsTT
CA645588536
NM_001276696.3:c.632_633delinsTG