Canonical Allele Identifier: PA2826448383
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 35573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Leu156Pro
CA129956
NM_001257970.1:c.467T>C