Canonical Allele Identifier: PA1139762747
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 940033
ClinVar RCV Id: RCV001209536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077015.2:p.Arg151Trp
CA8816425
NM_024110.4:c.451C>T