Canonical Allele Identifier: PA2828206927
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 68785
ClinVar RCV Id: RCV000059706 RCV000530376 RCV002262618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Ser200Asn
CA219920
NM_001366385.1:c.599G>A