Canonical Allele Identifier: PA2828206867
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393957
ClinVar RCV Id: RCV001884666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Glu126Gln
CA294858018
NM_001366385.1:c.376G>C