Canonical Allele Identifier: PA287698
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127812
ClinVar RCV Id: RCV000115723 RCV000533951 RCV000508084 RCV001255633 RCV003483477 RCV002288596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg158Cys
CA000225
NM_001126114.3:c.472C>T
CA645589032
NM_001126114.3:c.472_474delinsTGT
CA645589042
NM_001126114.3:c.471_472delinsTT