Canonical Allele Identifier: PA2580149117
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 1723537
ClinVar RCV Id: RCV002308811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Ala877Thr
CA390629643
NM_001080414.4:c.2629G>A