Canonical Allele Identifier: PA2825598930
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro72Ser
CA003069
NM_001126112.3:c.214C>T
CA2838032368
NM_001126112.3:c.214_215delinsAG