Canonical Allele Identifier: PA169051
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val143Met
CA000176
NM_000546.6:c.427G>A