Canonical Allele Identifier: PA2826561338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376576
ClinVar RCV Id: RCV000419348 RCV000420409 RCV000421679 RCV000421933 RCV000424052 RCV000426193 RCV000428210 RCV000430482 RCV000430655 RCV000431946 RCV000433046 RCV000437199 RCV000437018 RCV000438447 RCV000441834 RCV000442237 RCV000441879 RCV000492666 RCV000812726 RCV002289521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys199Arg
CA16603002
NM_001276696.3:c.595T>C