Canonical Allele Identifier: PA2826448439
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 955063
ClinVar RCV Id: RCV001227634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Arg220His
CA294858444
NM_001257970.1:c.659G>A