Canonical Allele Identifier: PA658679416
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 486555
ClinVar RCV Id: RCV000565161 RCV001731795 RCV002289837 RCV003767232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg283Pro
CA397836790
NM_001126114.3:c.848G>C