Canonical Allele Identifier: PA2826561029
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376606
ClinVar RCV Id: RCV000420789 RCV000417695 RCV000427175 RCV000417973 RCV000421853 RCV000423292 RCV000433943 RCV000437826 RCV000426502 RCV000433227 RCV000428674 RCV000429260 RCV000443785 RCV000438042 RCV000438407 RCV000439947 RCV000432550 RCV000440632 RCV000529132 RCV000445268 RCV000785555 RCV001023983 RCV001591055 RCV003983035 RCV004022216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.His140Arg
CA16603027
NM_001276696.3:c.419A>G