Canonical Allele Identifier: PA2826448425
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244899.1:p.Tyr205Asn
CA401337795
NM_001257970.1:c.613T>A