Canonical Allele Identifier: PA171511
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 158095
ClinVar RCV Id: RCV000145424 RCV000880885 RCV002505125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Arg735His
CA171510
NM_001080414.4:c.2204G>A