Canonical Allele Identifier: PA2826567478
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376583
ClinVar RCV Id: RCV000419235 RCV000420599 RCV000419912 RCV000423341 RCV000423990 RCV000425744 RCV000426441 RCV000431286 RCV000430590 RCV000434260 RCV000436480 RCV000437115 RCV000438476 RCV000441019 RCV000441335 RCV000441960 RCV000580293 RCV002521506
ClinVar Variation Id: 960924
ClinVar RCV Id: RCV001234533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys236Ser
CA16603007
NM_001276761.3:c.707G>C
CA397836943
NM_001276761.3:c.706T>A