Canonical Allele Identifier: PA2826561628
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 237956
ClinVar RCV Id: RCV000226273 RCV000235474 RCV000421276 RCV000436164 RCV000442318 RCV000442471 RCV000444806 RCV000418376 RCV000427734 RCV000429554 RCV000433180 RCV000437335 RCV000438489 RCV000439593 RCV000422340 RCV000423658 RCV000425549 RCV000426667 RCV000428909 RCV000431918 RCV000434324 RCV000492420 RCV000709768 RCV000767028 RCV001357626 RCV003463657 RCV003483584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg243Gln
CA10575441
NM_001276696.3:c.728G>A