Canonical Allele Identifier: PA2826561007
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376573
ClinVar RCV Id: RCV000419681 RCV000419497 RCV000421755 RCV000423671 RCV000425379 RCV000430429 RCV000430876 RCV000431070 RCV000431573 RCV000436082 RCV000436752 RCV000436236 RCV000438958 RCV000441815 RCV000444713 RCV000785469 RCV001023833 RCV001044520 RCV004022206
ClinVar Variation Id: 634759
ClinVar RCV Id: RCV000785487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys137Arg
CA16602999
NM_001276696.3:c.409T>C
CA913191047
NM_001276696.3:c.409_411delinsCGG