Canonical Allele Identifier: PA219921
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 68785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077015.2:p.Ser200Asn
CA219920
NM_024110.4:c.599G>A