Canonical Allele Identifier: PA916072883
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 684673
ClinVar RCV Id: RCV000845182
ClinVar Variation Id: 1461137
ClinVar RCV Id: RCV001965704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077015.2:p.Cys127Ser
CA401335743
NM_024110.4:c.379T>A
CA401335751
NM_024110.4:c.380G>C