Canonical Allele Identifier: PA645436159
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376607
ClinVar RCV Id: RCV000419975 RCV000420594 RCV000421045 RCV000421558 RCV000423857 RCV000425641 RCV000425896 RCV000428479 RCV000431364 RCV000429821 RCV000431267 RCV000436580 RCV000437195 RCV000436952 RCV000439103 RCV000441082 RCV000444017 RCV000444951 RCV000444976 RCV000815181 RCV001293868 RCV002264935 RCV002289527
ClinVar Variation Id: 406578
ClinVar RCV Id: RCV000464573 RCV000567952 RCV001527472 RCV003159559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His47Gln
CA16603028
NM_001126117.1:c.141T>G
CA16615708
NM_001126117.1:c.141T>A