Canonical Allele Identifier: PA2580149220
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 2320063
ClinVar RCV Id: RCV002893352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Thr1952Ser
CA390608750
NM_001080414.4:c.5855C>G
CA390608755
NM_001080414.4:c.5854A>T