Canonical Allele Identifier: PA658665639
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 473936
ClinVar RCV Id: RCV000540112 RCV003456414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Phe130Ile
CA366647263
NM_032415.6:c.388T>A