Canonical Allele Identifier: PA645436170
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376611
ClinVar RCV Id: RCV000420510 RCV000421224 RCV000421433 RCV000422328 RCV000426919 RCV000427172 RCV000427925 RCV000428125 RCV000431234 RCV000432547 RCV000433456 RCV000434884 RCV000437164 RCV000439058 RCV000438275 RCV000441519 RCV000444604 RCV000444694 RCV000443703 RCV001023982 RCV001861483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His47Pro
CA16603032
NM_001126117.1:c.140A>C