Canonical Allele Identifier: PA658665663
Gene: CARD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 473933
ClinVar RCV Id: RCV000534473 RCV001532094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115791.3:p.Glu1021Asp
CA4131863
NM_032415.6:c.3063G>C
CA366641180
NM_032415.6:c.3063G>T