Canonical Allele Identifier: PA2580149137
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2342103
ClinVar RCV Id: RCV002955896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Asn1108Thr
CA7309396
NM_001080414.4:c.3323A>C