Canonical Allele Identifier: PA2826562704
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Gly166Arg
CA397835820
NM_001276697.3:c.496G>A
CA397835825
NM_001276697.3:c.496G>C