Canonical Allele Identifier: PA645436058
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376640
ClinVar RCV Id: RCV000418846 RCV000419325 RCV000419958 RCV000421526 RCV000424514 RCV000425600 RCV000423715 RCV000430235 RCV000431352 RCV000435893 RCV000434196 RCV000435439 RCV000436541 RCV000439174 RCV000441608 RCV000440477 RCV000443101 RCV000633382 RCV003168617 RCV004022232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro19Arg
CA16603057
NM_001126117.1:c.56C>G