Canonical Allele Identifier: PA658817885
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 540972
ClinVar RCV Id: RCV000651145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Arg47His
CA4132883
NM_032415.6:c.140G>A