Canonical Allele Identifier: PA658679106
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Thr387Arg
CA287485465
NM_001126112.3:c.1160C>G