Canonical Allele Identifier: PA2828206938
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1493364
ClinVar RCV Id: RCV001984315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353314.1:p.Ala208Val
CA8816458
NM_001366385.1:c.623C>T