Canonical Allele Identifier: PA2825605042
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376579
ClinVar RCV Id: RCV000419559 RCV000423712 RCV000424356 RCV000430244 RCV000429187 RCV000431566 RCV000434352 RCV000439881 RCV000441578 RCV000440943 RCV000442629 RCV000662594 RCV001026200 RCV001325155
ClinVar Variation Id: 647334
ClinVar RCV Id: RCV000801823 RCV004028076
ClinVar Variation Id: 2124706
ClinVar RCV Id: RCV003039749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Cys242Ser
CA001776
NM_001126113.3:c.725G>C
CA16603004
NM_001126113.3:c.724T>A
CA2580094896
NM_001126113.3:c.725_726delinsCA