Canonical Allele Identifier: PA2827625869
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_001338716.1:p.Ser257Leu
CA9547799
NM_001351787.2:c.770C>T