Canonical Allele Identifier: PA2826560138
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Gly240Arg
CA397836876
NM_001276695.3:c.718G>C
CA397836877
NM_001276695.3:c.718G>A