Canonical Allele Identifier: PA2828191471
Gene: CARD8 HGNC NCBI
ClinVar RCV:
RCV003118760
ClinVar Variation:
2420235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352879.1:p.Ser256Leu
CA9547799
NM_001365950.1:c.767C>T