Canonical Allele Identifier: PA2741830630
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2577673
ClinVar RCV Id: RCV003325010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Asn699Lys
CA390631672
NM_001080414.4:c.2097C>G
CA390631674
NM_001080414.4:c.2097C>A