Canonical Allele Identifier: PA2826567537
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127824
ClinVar RCV Id: RCV000115739 RCV000122178 RCV000148912 RCV000200641 RCV000585912 RCV001357872 RCV000238755 RCV002477279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg244Cys
CA000457
NM_001276761.3:c.730C>T