ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828206893
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_001353314.1:p.Leu156Pro
CA129956
NM_001366385.1:c.467T>C