Canonical Allele Identifier: PA2825602811
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406608
ClinVar RCV Id: RCV000463583 RCV000774798 RCV002289605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Pro47Thr
CA16615959
NM_001126113.3:c.139C>A