Canonical Allele Identifier: PA169048
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142657
ClinVar RCV Id: RCV000132003 RCV000227179 RCV000409072 RCV000413546 RCV001354661 RCV001560552 RCV003474783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Val11Met
CA000176
NM_001126115.1:c.31G>A