Canonical Allele Identifier: PA2826567469
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376675
ClinVar RCV Id: RCV000419239 RCV000424200 RCV000425563 RCV000424885 RCV000431443 RCV000432106 RCV000434236 RCV000436477 RCV000443884 RCV000441480 RCV000443016 RCV001229449 RCV003168618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Val235Asp
CA16603089
NM_001276761.3:c.704T>A