Canonical Allele Identifier: PA2826562444
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376596
ClinVar RCV Id: RCV000418371 RCV000417655 RCV000417883 RCV000425994 RCV000427865 RCV000430718 RCV000436003 RCV000436185 RCV000438999 RCV000785257 RCV001362325 RCV002418243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Phe111Ile
CA16603018
NM_001276697.3:c.331T>A