Canonical Allele Identifier: PA2826561007
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376573
ClinVar Variation Id: 634759
ClinVar RCV Id: RCV000785487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys137Arg
CA16602999
NM_001276696.3:c.409T>C
CA913191047
NM_001276696.3:c.409_411delinsCGG