Canonical Allele Identifier: PA2825610498
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376687
ClinVar RCV Id: RCV000417798 RCV000420004 RCV000420142 RCV000422371 RCV000422197 RCV000429815 RCV000431076 RCV000430823 RCV000433089 RCV000431992 RCV000435010 RCV000436002 RCV000438238 RCV000439425 RCV000440468 RCV000440668 RCV000566866 RCV001215103 RCV003476013 RCV004022253 RCV000425148 RCV000444451 RCV000444634 RCV000785254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Tyr88His
CA002135
NM_001126115.1:c.262T>C