Canonical Allele Identifier: PA645489712
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 421663
ClinVar RCV Id: RCV000726904 RCV002526603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Arg75Gln
CA16618451
NM_032415.6:c.224G>A