Canonical Allele Identifier: PA2579953801
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Pro72Ser
CA003069
NM_000546.6:c.214C>T
CA2838032368
NM_000546.6:c.214_215delinsAG