Canonical Allele Identifier: PA2827246645
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 473938
ClinVar RCV Id: RCV000528697 RCV000788795 RCV002285361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311210.1:p.Arg30Trp
CA366647967
NM_001324281.3:c.88C>T