Canonical Allele Identifier: PA2826448371
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2002766
ClinVar RCV Id: RCV002824839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Gly144Glu
CA401336138
NM_001257970.1:c.431G>A