Canonical Allele Identifier: PA2826560488
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 572378
ClinVar RCV Id: RCV000693744 RCV001030739 RCV000771703 RCV002289972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro32Ser
CA397845838
NM_001276696.3:c.94C>T