ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA122231
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12365
ClinVar RCV Id:
RCV000013162
RCV000130147
RCV000144669
RCV000148909
RCV000154014
RCV000226657
RCV000419767
RCV000426990
RCV000426307
RCV000430925
RCV000428113
RCV000432120
RCV000437643
RCV000438107
RCV000421457
RCV000417419
RCV000432898
RCV000420452
RCV000442506
RCV000425581
RCV000436979
RCV000438801
RCV000442529
RCV000587017
RCV000588736
RCV000785316
RCV001270274
RCV001354825
RCV001642222
RCV002496337
RCV003162245
RCV003914832
RCV004540999
RCV003332080
RCV003460464
RCV004526594
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119588.1:p.Gly113Ser
CA000367
NM_001126116.1:c.337G>A