Canonical Allele Identifier: PA645436219
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376633
ClinVar RCV Id: RCV000419180 RCV000420755 RCV000422070 RCV000424933 RCV000428827 RCV000430366 RCV000437791 RCV000440633 RCV000535418 RCV000561306 RCV000785551 RCV001270270 RCV004022229 RCV000431014 RCV000436915 RCV000439886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Leu62Arg
CA16044097
NM_001126117.1:c.185T>G