Canonical Allele Identifier: PA2826560999
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182963
ClinVar RCV Id: RCV000161065 RCV000810785 RCV002288703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg136Leu
CA000252
NM_001276696.3:c.407G>T