Canonical Allele Identifier: PA2827625451
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1145399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338713.1:p.Pro281Leu
CA9547786
NM_001351784.2:c.842C>T