Canonical Allele Identifier: PA2825598989
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790682
ClinVar RCV Id: RCV002450234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro80Leu
CA397845543
NM_001126112.3:c.239C>T