Canonical Allele Identifier: PA2580149196
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2067617
ClinVar RCV Id: RCV002954046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Gly1721Arg
CA7308720
NM_001080414.4:c.5161G>A
CA390610750
NM_001080414.4:c.5161G>C