Canonical Allele Identifier: PA2826561332
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376575
ClinVar RCV Id: RCV000418923 RCV000419485 RCV000423226 RCV000424531 RCV000425465 RCV000425867 RCV000424302 RCV000429749 RCV000432222 RCV000434344 RCV000435732 RCV000434584 RCV000440842 RCV000439773 RCV000441115 RCV000442527 RCV000442617 RCV001067780 RCV001523834 RCV001551247 RCV002289520
ClinVar Variation Id: 485039
ClinVar RCV Id: RCV000565464 RCV003509567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys199Ser
CA16603001
NM_001276696.3:c.596G>C
CA397839198
NM_001276696.3:c.595T>A