Canonical Allele Identifier: PA2827625649
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420235
ClinVar RCV Id: RCV003118760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338715.1:p.Ser250Leu
CA9547799
NM_001351786.2:c.749C>T