Canonical Allele Identifier: PA645435959
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376659
ClinVar RCV Id: RCV000417919 RCV000419006 RCV000417824 RCV000423005 RCV000423789 RCV000424978 RCV000425389 RCV000427957 RCV000426071 RCV000428608 RCV000432620 RCV000433722 RCV000434763 RCV000435036 RCV000440221 RCV000438637 RCV000441023 RCV000441861 RCV000442220 RCV000492764 RCV000709402 RCV002289536 RCV002502456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg282Pro
CA16603074
NM_001126114.3:c.845G>C