Canonical Allele Identifier: PA2825601110
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376015
ClinVar RCV Id: RCV000420349 RCV000422597 RCV000423288 RCV000424367 RCV000425028 RCV000431816 RCV000433555 RCV000430687 RCV000440254 RCV000440948 RCV000441532 RCV000426063 RCV000444945 RCV000445262 RCV000432872 RCV000438147 RCV000444506 RCV001311109 RCV002392945 RCV004022197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Arg249Thr
CA16602484
NM_001126112.3:c.746G>C