ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827246701
Gene: CARD11
HGNC
NCBI
Linked Data
ClinVar Variation Id:
48648
ClinVar RCV Id:
RCV000041969
RCV001057931
RCV002243689
RCV002512055
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001311210.1:p.Gly123Ser
CA143685
NM_001324281.3:c.367G>A