Canonical Allele Identifier: PA185999
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 183144
ClinVar RCV Id: RCV000162028 RCV001850281
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Gly123Asp
CA185998
NM_032415.6:c.368G>A