Canonical Allele Identifier: PA2826149973
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2409418
ClinVar RCV Id: RCV003778645 RCV004245335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171829.1:p.Phe354Leu
CA9547804
NM_001184900.3:c.1062C>G
CA406665356
NM_001184900.3:c.1062C>A
CA406665360
NM_001184900.3:c.1060T>C