Canonical Allele Identifier: PA2828207485
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 527870
ClinVar RCV Id: RCV000632892 RCV002263853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Gly881Arg
CA8817398
NM_001366385.1:c.2641G>A
CA401356395
NM_001366385.1:c.2641G>C