Canonical Allele Identifier: PA2826149994
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 999304
ClinVar RCV Id: RCV001295285
ClinVar Variation Id: 2829221
ClinVar RCV Id: RCV003686236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171829.1:p.Gln415His
CA406664712
NM_001184900.3:c.1245A>T
CA406664714
NM_001184900.3:c.1245A>C