Canonical Allele Identifier: PA658679172
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Met66Ile
CA397846006
NM_001126114.3:c.198G>A
CA397846013
NM_001126114.3:c.198G>T
CA397846016
NM_001126114.3:c.198G>C