Canonical Allele Identifier: PA2826149791
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 252559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171829.1:p.Val44Ile
CA10586039
NM_001184900.3:c.130G>A