ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826561626
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
140821
ClinVar RCV Id:
RCV000129010
RCV000422367
RCV000435503
RCV000437895
RCV000440653
RCV000422134
RCV000422747
RCV000430047
RCV000437219
RCV000442540
RCV000419993
RCV000425179
RCV000430393
RCV000431764
RCV000432433
RCV000442627
RCV000419333
RCV000427647
RCV000440446
RCV000445294
RCV000785299
RCV001380073
RCV002288620
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Arg243Gly
CA000453
NM_001276696.3:c.727C>G