ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825604162
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
245851
ClinVar RCV Id:
RCV000235329
RCV000422641
RCV000426785
RCV000438017
RCV000439251
RCV000439855
RCV000440307
RCV000442812
RCV000417778
RCV000418929
RCV000785238
RCV000421969
RCV000427794
RCV000433090
RCV000433333
RCV000434308
RCV000429015
RCV000435664
RCV000444463
RCV000418017
RCV000423061
RCV000424499
RCV000429222
RCV000439625
RCV000574439
RCV000704159
RCV003152698
RCV002268012
RCV003483596
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.Arg175Cys
CA002442
NM_001126113.3:c.523C>T