Canonical Allele Identifier: PA2826561570
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376583
ClinVar Variation Id: 960924
ClinVar RCV Id: RCV001234533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys236Ser
CA16603007
NM_001276696.3:c.707G>C
CA397836943
NM_001276696.3:c.706T>A