Canonical Allele Identifier: PA2826566007
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141141
ClinVar RCV Id: RCV000129516 RCV000418257 RCV000429146 RCV000436807 RCV000425885 RCV000426980 RCV000428043 RCV000434395 RCV000435472 RCV000436592 RCV000418481 RCV000431187 RCV000433596 RCV000441016 RCV000442068 RCV000423760 RCV000423959 RCV000438583 RCV000442813 RCV000633367 RCV003237737 RCV002288626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asp242Gly
CA000450
NM_001276760.3:c.725A>G