Canonical Allele Identifier: PA2573065019
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 1335158
ClinVar RCV Id: RCV001815766 RCV003163957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Arg1701Gln
CA7308733
NM_001080414.4:c.5102G>A