Canonical Allele Identifier: PA2826561774
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492627
ClinVar RCV Id: RCV000584424 RCV002289878 RCV003767316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro279Leu
CA397835952
NM_001276696.3:c.836C>T