Canonical Allele Identifier: PA2580149113
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 1927830
ClinVar RCV Id: RCV002610078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Ala841Val
CA7309628
NM_001080414.4:c.2522C>T