Canonical Allele Identifier: PA2826448423
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072819
ClinVar RCV Id: RCV002967395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.His204Arg
CA401337774
NM_001257970.1:c.611A>G