Canonical Allele Identifier: PA2829790506
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1145399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055774.2:p.Pro336Leu
CA9547786
NM_014959.5:c.1007C>T