Canonical Allele Identifier: PA2826567498
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376643
ClinVar RCV Id: RCV000419944 RCV000418460 RCV000425201 RCV000425878 RCV000429149 RCV000429755 RCV000433992 RCV000435065 RCV000436548 RCV000437214 RCV000440415 RCV000442861 RCV000442983 RCV000626445 RCV000785511 RCV002429348 RCV002524698 RCV004022234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro239Thr
CA16603060
NM_001276761.3:c.715C>A