Canonical Allele Identifier: PA916031161
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 252559
ClinVar RCV Id: RCV000238764 RCV001263446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338711.1:p.Val44Ile
CA10586039
NM_001351782.2:c.130G>A