Canonical Allele Identifier: PA166690
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141881
ClinVar RCV Id: RCV000130578 RCV000425504 RCV000432429 RCV000434278 RCV000440994 RCV000431276 RCV000432948 RCV000435888 RCV000443796 RCV000433563 RCV000435249 RCV000444809 RCV000417537 RCV000418238 RCV000423307 RCV000424980 RCV000426167 RCV002514731 RCV003237740 RCV003460931 RCV004019741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Arg249Trp
CA000389
NM_000546.6:c.745A>T