Canonical Allele Identifier: PA915968064
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 791504
ClinVar RCV Id: RCV000974478 RCV004029982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Val1766Met
CA7308680
NM_001080414.4:c.5296G>A