Canonical Allele Identifier: PA2826567483
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428893
ClinVar RCV Id: RCV000492584 RCV000785453 RCV000705570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala237Pro
CA397836931
NM_001276761.3:c.709G>C