Canonical Allele Identifier: PA915979071
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 821636
ClinVar RCV Id: RCV001016237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro89Thr
CA397845257
NM_001126114.3:c.265C>A