Canonical Allele Identifier: PA157839
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 133802
ClinVar RCV Id: RCV000120453 RCV000804742 RCV001532093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Ala1047Thr
CA157838
NM_032415.6:c.3139G>A