Canonical Allele Identifier: PA2580149139
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2418437
ClinVar RCV Id: RCV003121186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Ala1116Thr
CA7309389
NM_001080414.4:c.3346G>A