Canonical Allele Identifier: PA2741830632
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2591616
ClinVar RCV Id: RCV003341072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Arg717His
CA7309733
NM_001080414.4:c.2150G>A