Canonical Allele Identifier: PA658654746
Gene: TP53RK HGNC NCBI

Linked Data

ClinVar Variation Id: 444883
ClinVar RCV Id: RCV000513223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_291028.3:p.Arg243Leu
CA409269086
NM_033550.4:c.728G>T