ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826563495
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376623
ClinVar RCV Id:
RCV000420356
RCV000420641
RCV000424525
RCV000427837
RCV000435232
RCV000437646
RCV000442535
RCV000458707
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.Ile96Thr
CA16603043
NM_001276698.3:c.287T>C