ClinGen Allele Registry
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Canonical Allele Identifier:
PA193067
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
185366
ClinVar RCV:
RCV000165315
RCV000419701
RCV000420523
RCV000421145
RCV000421777
RCV000422830
RCV000426960
RCV000427615
RCV000428359
RCV000430839
RCV000431198
RCV000432479
RCV000433537
RCV000437609
RCV000437660
RCV000438323
RCV000438373
RCV000439007
RCV000441921
RCV000443734
RCV000444673
RCV000697802
RCV000785542
RCV004019975
ClinVar Variation:
185822
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119587.1:p.His61Leu
CA000276
NM_001126115.1:c.182A>T