Canonical Allele Identifier: PA2573285046
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372992
ClinVar RCV Id: RCV001874984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077015.2:p.Ser202Leu
CA8816456
NM_024110.4:c.605C>T