Canonical Allele Identifier: PA2826565780
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12365
ClinVar RCV Id: RCV000013162 RCV000130147 RCV000144669 RCV000148909 RCV000154014 RCV000226657 RCV000419767 RCV000426990 RCV000426307 RCV000430925 RCV000428113 RCV000432120 RCV000437643 RCV000438107 RCV000421457 RCV000417419 RCV000432898 RCV000420452 RCV000442506 RCV000425581 RCV000436979 RCV000438801 RCV000442529 RCV000587017 RCV000588736 RCV000785316 RCV001270274 RCV001354825 RCV001642222 RCV002496337 RCV003162245 RCV003914832 RCV004540999 RCV003332080 RCV003460464 RCV004526594
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Gly206Ser
CA000367
NM_001276760.3:c.616G>A