Canonical Allele Identifier: PA2825617145
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1734453
ClinVar RCV Id: RCV002349223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Thr86Ala
CA397844193
NM_001126118.1:c.256A>G