Canonical Allele Identifier: PA2827625869
Gene: CARD8 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338716.1:p.Ser257Leu
CA9547799
NM_001351787.2:c.770C>T