Canonical Allele Identifier: PA2826150711
Gene: CARD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1145399
ClinVar RCV Id: RCV001484252 RCV003938867
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171832.1:p.Pro386Leu
CA9547786
NM_001184903.1:c.1157C>T