Canonical Allele Identifier: PA287829
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127823
ClinVar RCV Id: RCV000115737 RCV000205433 RCV000213058 RCV000662441 RCV001358724 RCV001358329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Arg267Gln
CA000424
NM_001126112.3:c.800G>A