Canonical Allele Identifier: PA658654673
Gene: CCDC88C HGNC NCBI

Linked Data

ClinVar Variation Id: 444336
ClinVar RCV Id: RCV000513515 RCV000765186 RCV001849184 RCV002524960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073883.2:p.Pro2009Leu
CA7308526
NM_001080414.4:c.6026C>T