Canonical Allele Identifier: PA269899
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 133280
ClinVar RCV Id: RCV000119793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ala90Val
CA000150
NM_001126118.1:c.269C>T