ClinGen Allele Registry
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Canonical Allele Identifier:
PA645475678
Gene: CC2D2A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
281114
ClinVar RCV Id:
RCV000373113
RCV000440940
RCV001088602
RCV004542970
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001073991.2:p.Met938Thr
CA2864006
NM_001080522.2:c.2813T>C