Canonical Allele Identifier: PA2828206932
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072819
ClinVar RCV Id: RCV002967395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.His204Arg
CA401337774
NM_001366385.1:c.611A>G