Canonical Allele Identifier: PA2825613705
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230253
ClinVar RCV Id: RCV000219834 RCV000422303 RCV000422821 RCV000429221 RCV000439901 RCV000427307 RCV000428586 RCV000434177 RCV000417894 RCV000418531 RCV000439516 RCV000440686 RCV000423159 RCV000423468 RCV000424394 RCV000443712 RCV000424119 RCV000445266 RCV000430044 RCV000433237 RCV000435726 RCV000433865 RCV000443630 RCV000435101 RCV000437940 RCV000445145 RCV000991149 RCV003475005 RCV004020650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Arg116Leu
CA10580924
NM_001126116.1:c.347G>T
CA645588548
NM_001126116.1:c.347_348delinsTT