Canonical Allele Identifier: PA2826565116
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2687698
ClinVar RCV Id: RCV003484943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro89Ser
CA397843904
NM_001276760.3:c.265C>T