Canonical Allele Identifier: PA2741830637
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 3037271
ClinVar RCV Id: RCV004550941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Arg756Cys
CA7309704
NM_001080414.4:c.2266C>T