Canonical Allele Identifier: PA2580149094
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2169000
ClinVar RCV Id: RCV003082852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Arg697Cys
CA7309749
NM_001080414.4:c.2089C>T