Canonical Allele Identifier: PA166911
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141956
ClinVar RCV Id: RCV000130694 RCV001303642 RCV002288640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ala83Glu
CA000082
NM_001126112.3:c.248C>A