Canonical Allele Identifier: PA645392237
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 376980
ClinVar RCV Id: RCV000443675 RCV000765189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Arg197Gln
CA7310199
NM_001080414.4:c.590G>A