Canonical Allele Identifier: PA169185
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142702
ClinVar RCV Id: RCV000132069 RCV001050775 RCV002288653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Thr172Ala
CA000493
NM_001126115.1:c.514A>G