Canonical Allele Identifier: PA169128
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142689
ClinVar RCV Id: RCV000132048 RCV001364215 RCV001559782 RCV002288651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Asp7His
CA000065
NM_001126113.3:c.19G>C