Canonical Allele Identifier: PA2826567702
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480952
ClinVar RCV Id: RCV000566077 RCV001217424 RCV003476325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly286Glu
CA397835817
NM_001276761.3:c.857G>A