Canonical Allele Identifier: PA2826565389
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 245851
ClinVar RCV Id: RCV000235329 RCV000422641 RCV000426785 RCV000438017 RCV000439251 RCV000439855 RCV000440307 RCV000442812 RCV000417778 RCV000418929 RCV000785238 RCV000421969 RCV000427794 RCV000433090 RCV000433333 RCV000434308 RCV000429015 RCV000435664 RCV000444463 RCV000418017 RCV000423061 RCV000424499 RCV000429222 RCV000439625 RCV000574439 RCV000704159 RCV003152698 RCV002268012 RCV003483596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg136Cys
CA002442
NM_001276760.3:c.406C>T