Canonical Allele Identifier: PA287772
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127818
ClinVar RCV Id: RCV000115729 RCV000473040 RCV000563913 RCV001257499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg70Cys
CA000288
NM_001126115.1:c.208C>T