Canonical Allele Identifier: PA2580149231
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2083166
ClinVar RCV Id: RCV002999696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Val2004Ile
CA7308532
NM_001080414.4:c.6010G>A