Canonical Allele Identifier: PA2826150703
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_001171832.1:p.Ser362Leu
CA9547799
NM_001184903.1:c.1085C>T