Canonical Allele Identifier: PA157843
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 133804
ClinVar RCV Id: RCV000120455 RCV000704118 RCV001532097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Asn191Ser
CA157842
NM_032415.6:c.572A>G