Canonical Allele Identifier: PA2828206937
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2932260
ClinVar RCV Id: RCV003795474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Asn207Asp
CA401337835
NM_001366385.1:c.619A>G