Canonical Allele Identifier: PA2825598932
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450744
ClinVar RCV Id: RCV003171492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro72_Val73delinsArgMet
CA913187840
NM_001126112.3:c.215_217delinsGCA