Canonical Allele Identifier: PA2825598971
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718262
ClinVar RCV Id: RCV002304859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro77Ala
CA397845624
NM_001126112.3:c.229C>G