Canonical Allele Identifier: PA2826559402
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142766
ClinVar RCV Id: RCV000132156 RCV000168122 RCV000583667 RCV000677669 RCV000755703 RCV001270267 RCV001255632 RCV003462034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro113Leu
CA000204
NM_001276695.3:c.338C>T
CA645589087
NM_001276695.3:c.337_338delinsTT