Canonical Allele Identifier: PA645489847
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 421704
ClinVar RCV Id: RCV000499590 RCV000484392 RCV003766695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Arg975Trp
CA16618450
NM_032415.6:c.2923C>T