Canonical Allele Identifier: PA658654745
Gene: TP53RK HGNC NCBI

Linked Data

ClinVar Variation Id: 444881
ClinVar RCV Id: RCV000513568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_291028.3:p.Thr81Arg
CA409258575
NM_033550.4:c.242C>G