Canonical Allele Identifier: PA2741830694
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2694237
ClinVar RCV Id: RCV003544065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Ser1765Thr
CA390610217
NM_001080414.4:c.5294G>C