Canonical Allele Identifier: PA645436259
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376651
ClinVar RCV Id: RCV000417479 RCV000419627 RCV000420272 RCV000421648 RCV000421524 RCV000425630 RCV000424254 RCV000426157 RCV000426799 RCV000428823 RCV000428146 RCV000431481 RCV000430949 RCV000432206 RCV000432863 RCV000436862 RCV000438186 RCV000437472 RCV000438834 RCV000438677 RCV000444193 RCV000444980 RCV002356518 RCV002524699 RCV004022237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg81Gly
CA16603068
NM_001126117.1:c.241C>G