ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826559390
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
133282
ClinVar RCV Id:
RCV000119795
RCV002514608
RCV004019663
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263624.1:p.Thr111_Pro114del
CA000194
NM_001276695.3:c.331_342del