Canonical Allele Identifier: PA2826566006
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182968
ClinVar RCV Id: RCV000161072 RCV000215048 RCV000418100 RCV000428503 RCV000426125 RCV000434194 RCV000432892 RCV000435682 RCV000435739 RCV000440916 RCV000442104 RCV000417569 RCV000423186 RCV000425401 RCV000423894 RCV000431328 RCV000433464 RCV000438736 RCV000443096 RCV000441595 RCV000799325 RCV002288706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asp242Val
CA000452
NM_001276760.3:c.725A>T