Canonical Allele Identifier: PA2826565986
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376645
ClinVar RCV Id: RCV000419216 RCV000417926 RCV000420739 RCV000422309 RCV000426460 RCV000427997 RCV000430547 RCV000433017 RCV000437350 RCV000438674 RCV000437992 RCV000439356 RCV000441270 RCV000567850 RCV000688854 RCV000785477 RCV001584114 RCV004022235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro239Ala
CA16603062
NM_001276760.3:c.715C>G