Canonical Allele Identifier: PA193064
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185822
ClinVar RCV Id: RCV000165315 RCV000422830 RCV000431198 RCV000433537 RCV000427615 RCV000432479 RCV000419701 RCV000421145 RCV000437609 RCV000426960 RCV000441921 RCV000430839 RCV000443734 RCV000420523 RCV000421777 RCV000428359 RCV000437660 RCV000438323 RCV000438373 RCV000439007 RCV000444673 RCV000697802 RCV000785542 RCV004019975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.His193Leu
CA000276
NM_001126112.3:c.578A>T