Canonical Allele Identifier: PA2826566101
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 481049
ClinVar RCV Id: RCV000574619 RCV002289805 RCV001858158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro262Leu
CA397836344
NM_001276760.3:c.785C>T