ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA338198
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
216077
ClinVar RCV Id:
RCV000198789
RCV000418938
RCV000423911
RCV000434089
RCV000421097
RCV000421751
RCV000439388
RCV000441624
RCV000434805
RCV000442071
RCV000429852
RCV000436603
RCV000438726
RCV000419621
RCV000428484
RCV000429211
RCV000437301
RCV000487386
RCV000785324
RCV001024600
RCV001271054
RCV002288812
RCV003474953
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119587.1:p.Ile63Thr
CA002232
NM_001126115.1:c.188T>C