Canonical Allele Identifier: PA2826448443
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 3137305
ClinVar RCV Id: RCV004427137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Gln223Arg
CA401338184
NM_001257970.1:c.668A>G