Canonical Allele Identifier: PA658679262
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458559
ClinVar RCV Id: RCV000544531
ClinVar Variation Id: 826894
ClinVar RCV Id: RCV001026129
ClinVar Variation Id: 1504304
ClinVar RCV Id: RCV002028697 RCV003170564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ser240Arg
CA397839103
NM_001126114.3:c.720T>G
CA397839114
NM_001126114.3:c.720T>A
CA397839143
NM_001126114.3:c.718A>C