Canonical Allele Identifier: PA2828206931
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372992
ClinVar RCV Id: RCV001874984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Ser202Leu
CA8816456
NM_001366385.1:c.605C>T