Canonical Allele Identifier: PA2826561001
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376649
ClinVar RCV Id: RCV000419625 RCV000421238 RCV000421436 RCV000420706 RCV000420923 RCV000424235 RCV000425355 RCV000426938 RCV000428548 RCV000430584 RCV000430740 RCV000430935 RCV000432831 RCV000432105 RCV000436078 RCV000436759 RCV000437498 RCV000438570 RCV000441260 RCV000444111 RCV000443278 RCV000459914 RCV000444080 RCV000573315 RCV000785486 RCV001584115 RCV002289532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg136Gly
CA16603066
NM_001276696.3:c.406C>G