Canonical Allele Identifier: PA2826564110
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376661
ClinVar Variation Id: 428895
ClinVar Variation Id: 2020649
ClinVar RCV Id: RCV002857438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Ser56Arg
CA16603076
NM_001276699.3:c.168T>G
CA397839990
NM_001276699.3:c.168T>A
CA397840019
NM_001276699.3:c.166A>C