Canonical Allele Identifier: PA2826567697
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 420950
ClinVar RCV Id: RCV000478385 RCV000555965 RCV000573045 RCV002289633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Asp285His
CA16620612
NM_001276761.3:c.853G>C