Canonical Allele Identifier: PA2826565608
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182965
ClinVar RCV Id: RCV000161067 RCV000168150 RCV000421726 RCV000421819 RCV000424101 RCV000431843 RCV000428263 RCV000432944 RCV000443170 RCV000444190 RCV000426366 RCV000436614 RCV000438503 RCV000583984 RCV000561534 RCV000663213 RCV000785523 RCV003474837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Val177Met
CA000308
NM_001276760.3:c.529G>A