Canonical Allele Identifier: PA2826566579
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2029805
ClinVar RCV Id: RCV002863871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala44Thr
CA397845502
NM_001276761.3:c.130G>A