Canonical Allele Identifier: PA2826559398
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12369
ClinVar RCV Id: RCV000013168 RCV000130617 RCV000417493 RCV000418145 RCV000425139 RCV000429500 RCV000423161 RCV000424222 RCV000428384 RCV000428836 RCV000442802 RCV000437544 RCV000691152 RCV000433405 RCV000435159 RCV000443817 RCV000520731 RCV000422094 RCV001257524 RCV000434485 RCV000439740 RCV000440812 RCV002288486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro112Thr
CA000198
NM_001276695.3:c.334C>A