Canonical Allele Identifier: PA2825598784
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 231133
ClinVar RCV Id: RCV000219898 RCV000702036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asp49Gly
CA003170
NM_001126112.3:c.146A>G