Canonical Allele Identifier: PA2580149112
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2218054
ClinVar RCV Id: RCV002661363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Ala828Val
CA7309637
NM_001080414.4:c.2483C>T