Canonical Allele Identifier: PA2826561076
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 646725
ClinVar RCV Id: RCV000801073 RCV001024409 RCV002290443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro151Ser
CA397840839
NM_001276696.3:c.451C>T