Canonical Allele Identifier: PA1139762819
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 956894
ClinVar RCV Id: RCV001229780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077015.2:p.Arg218His
CA294858421
NM_024110.4:c.653G>A