Canonical Allele Identifier: PA2580149096
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2063707
ClinVar RCV Id: RCV002948665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Arg710Cys
CA7309740
NM_001080414.4:c.2128C>T