Canonical Allele Identifier: PA2828207486
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039897
ClinVar RCV Id: RCV001343455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Gly882Asp
CA401356401
NM_001366385.1:c.2645G>A