Canonical Allele Identifier: PA203897
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 203461
ClinVar RCV Id: RCV000185616 RCV001390618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Cys49Tyr
CA203896
NM_032415.6:c.146G>A