Canonical Allele Identifier: PA2827247241
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 421704
ClinVar RCV Id: RCV000499590 RCV000484392 RCV003766695
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311210.1:p.Arg975Trp
CA16618450
NM_001324281.3:c.2923C>T