Canonical Allele Identifier: PA2828206913
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 68783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Arg179His
CA219916
NM_001366385.1:c.536G>A