Canonical Allele Identifier: PA2826149980
Gene: CARD8 HGNC NCBI
ClinVar RCV:
RCV003118760
ClinVar Variation:
2420235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171829.1:p.Ser362Leu
CA9547799
NM_001184900.3:c.1085C>T