Canonical Allele Identifier: PA2826561936
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2687634
ClinVar RCV Id: RCV003484383
ClinVar Variation Id: 3074246
ClinVar RCV Id: RCV004012788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His20del
CA645588925
NM_001276697.3:c.57_59del
CA2825002607
NM_001276697.3:c.58_60del