Canonical Allele Identifier: PA2826561691
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 100816
ClinVar RCV Id: RCV000087174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.His257Arg
CA000476
NM_001276696.3:c.770A>G