Canonical Allele Identifier: PA2825612389
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376565
ClinVar RCV Id: RCV000419723 RCV000420817 RCV000418678 RCV000423623 RCV000425407 RCV000432161 RCV000430017 RCV000437414 RCV000431037 RCV000436190 RCV000440220 RCV000441312 RCV001861481 RCV002328907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Cys9Arg
CA16602991
NM_001126116.1:c.25T>C