ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA113192
Gene: CARD14
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000029229
RCV000845186
RCV001852578
ClinVar Variation:
35573
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_077015.2:p.Leu156Pro
CA129956
NM_024110.4:c.467T>C