Canonical Allele Identifier: PA2826566567
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790682
ClinVar RCV Id: RCV002450234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro41Leu
CA397845543
NM_001276761.3:c.122C>T