Canonical Allele Identifier: PA2826560337
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Gly286Arg
CA397835820
NM_001276695.3:c.856G>A
CA397835825
NM_001276695.3:c.856G>C