Canonical Allele Identifier: PA2827247267
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 473933
ClinVar RCV Id: RCV000534473 RCV001532094
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311210.1:p.Glu1021Asp
CA4131863
NM_001324281.3:c.3063G>C
CA366641180
NM_001324281.3:c.3063G>T