Canonical Allele Identifier: PA196611
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 187052
ClinVar RCV Id: RCV000166739 RCV000417885 RCV000430982 RCV000434903 RCV000426124 RCV000441262 RCV000444147 RCV000420162 RCV000432709 RCV000420721 RCV000435516 RCV000424608 RCV000425235 RCV000433509 RCV000443587 RCV001850353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Tyr31Asp
CA000239
NM_001126115.1:c.91T>G