Canonical Allele Identifier: PA106989
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12355
ClinVar Variation Id: 861760
ClinVar RCV Id: RCV001068346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Gly245Asp
CA000371
NM_000546.6:c.734G>A
CA916081933
NM_000546.6:c.734_735delinsAT