Canonical Allele Identifier: PA2499250719
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1145399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338711.1:p.Pro386Leu
CA9547786
NM_001351782.2:c.1157C>T