Canonical Allele Identifier: PA094715
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 48648
ClinVar RCV Id: RCV000041969 RCV001057931 RCV002243689 RCV002512055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Gly123Ser
CA143685
NM_032415.6:c.367G>A