Canonical Allele Identifier: PA2826149987
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1145399
ClinVar RCV Id: RCV001484252 RCV003938867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171829.1:p.Pro386Leu
CA9547786
NM_001184900.3:c.1157C>T