Canonical Allele Identifier: PA2827420060
Gene: CCDC180 HGNC NCBI

Linked Data

ClinVar Variation Id: 3138939
ClinVar RCV Id: RCV004435299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334939.2:p.Tyr767Ser
CA5145552
NM_001348010.4:c.2300A>C