Canonical Allele Identifier: PA2826560469
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Met27Ile
CA397846006
NM_001276696.3:c.81G>A
CA397846013
NM_001276696.3:c.81G>T
CA397846016
NM_001276696.3:c.81G>C