Canonical Allele Identifier: PA2580149190
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2365740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Pro1689Arg
CA7308743
NM_001080414.4:c.5066C>G