Canonical Allele Identifier: PA193949
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186132
ClinVar RCV Id: RCV000165667 RCV000819967 RCV002288749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Thr102Ile
CA000098
NM_001126112.3:c.305C>T