Canonical Allele Identifier: PA2826561801
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 246069
ClinVar RCV Id: RCV000235861
ClinVar Variation Id: 1361331
ClinVar RCV Id: RCV001874295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Tyr288Ter
CA645587349
NM_001276696.3:c.863_864insAA