Canonical Allele Identifier: PA645435856
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376605
ClinVar Variation Id: 458566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Gly266Arg
CA16603026
NM_001126114.3:c.796G>C
CA397837142
NM_001126114.3:c.796G>A
CA645588448
NM_001126114.3:c.795_796delinsAA