Canonical Allele Identifier: PA2826567490
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 421804
ClinVar RCV Id: RCV000480494 RCV000819627 RCV002248705 RCV002431408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys238Arg
CA16620617
NM_001276761.3:c.712T>C