Canonical Allele Identifier: PA2826565858
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528269
ClinVar RCV Id: RCV000633389 RCV001026685 RCV002289933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Thr217Pro
CA397837741
NM_001276760.3:c.649A>C