Canonical Allele Identifier: PA2825610900
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 237954
ClinVar RCV Id: RCV000229442 RCV000420292 RCV000421633 RCV000425773 RCV000430314 RCV000434831 RCV000431663 RCV000432304 RCV000432999 RCV000436850 RCV000438849 RCV000445077 RCV000418894 RCV000419610 RCV000426089 RCV000435488 RCV000436124 RCV000441018 RCV000444130 RCV000444805 RCV000420936 RCV000424795 RCV000425414 RCV000430964 RCV000441674 RCV000443867 RCV002378977 RCV004020765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg116Pro
CA10583676
NM_001126115.1:c.347G>C