Canonical Allele Identifier: PA2827246709
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 48647
ClinVar RCV Id: RCV000041968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311210.1:p.Glu134Gly
CA143684
NM_001324281.3:c.401A>G