Canonical Allele Identifier: PA2826448366
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 31609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Glu138Ala
CA129844
NM_001257970.1:c.413A>C