Canonical Allele Identifier: PA2826448392
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1510314
ClinVar RCV Id: RCV002011673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Arg166His
CA294858200
NM_001257970.1:c.497G>A