Canonical Allele Identifier: PA338282
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216472
ClinVar RCV Id: RCV000198910 RCV000236248 RCV000492120 RCV001723772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg158Cys
CA001448
NM_001126115.1:c.472C>T