Canonical Allele Identifier: PA157819
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 133792
ClinVar RCV Id: RCV000120443 RCV000707585 RCV002492420 RCV004019674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Arg707Cys
CA157818
NM_032415.6:c.2119C>T