ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826448369
Gene: CARD14
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
40292
ClinVar RCV:
RCV000024312
RCV000059701
ClinVar Variation:
31608
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001244899.1:p.Glu142Gly
CA129843
NM_001257970.1:c.425A>G