Canonical Allele Identifier: PA2827626090
Gene: CARD8 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338717.1:p.Ser312Leu
CA9547799
NM_001351788.2:c.935C>T