Canonical Allele Identifier: PA2580149098
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 1878296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Ala724Val
CA7309730
NM_001080414.4:c.2171C>T