Canonical Allele Identifier: PA2826150232
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2420235
ClinVar RCV Id: RCV003118760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171830.1:p.Ser312Leu
CA9547799
NM_001184901.1:c.935C>T