Canonical Allele Identifier: PA658817657
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 525443
ClinVar RCV Id: RCV000629502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Ser11Cys
CA8813355
NM_017950.4:c.32C>G