Canonical Allele Identifier: PA2826559734
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376650
ClinVar RCV Id: RCV000417467 RCV000418814 RCV000418608 RCV000421737 RCV000422458 RCV000422684 RCV000428488 RCV000428624 RCV000428841 RCV000427240 RCV000427500 RCV000433789 RCV000432738 RCV000435387 RCV000435132 RCV000437481 RCV000438469 RCV000439587 RCV000439979 RCV000443648 RCV000444469 RCV000445195 RCV001371092 RCV004022236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg174Leu
CA16603067
NM_001276695.3:c.521G>T