Canonical Allele Identifier: PA2741830642
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2715068
ClinVar RCV Id: RCV003553118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Ala871Val
CA7309604
NM_001080414.4:c.2612C>T