Canonical Allele Identifier: PA2826448359
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 684673
ClinVar RCV Id: RCV000845182
ClinVar Variation Id: 1461137
ClinVar RCV Id: RCV001965704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Cys127Ser
CA401335743
NM_001257970.1:c.379T>A
CA401335751
NM_001257970.1:c.380G>C