Canonical Allele Identifier: PA2826561789
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2450758
ClinVar RCV Id: RCV003177183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Asp285Glu
CA397835829
NM_001276696.3:c.855T>A
CA397835833
NM_001276696.3:c.855T>G