ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826562533
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376659
ClinVar RCV Id:
RCV000417919
RCV000419006
RCV000417824
RCV000423005
RCV000423789
RCV000424978
RCV000425389
RCV000427957
RCV000426071
RCV000428608
RCV000432620
RCV000433722
RCV000434763
RCV000435036
RCV000440221
RCV000438637
RCV000441023
RCV000441861
RCV000442220
RCV000492764
RCV000709402
RCV002289536
RCV002502456
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263626.1:p.Arg123Pro
CA16603074
NM_001276697.3:c.368G>C