Canonical Allele Identifier: PA2826327316
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 414637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Ile933Ser
CA8814346
NM_001243342.2:c.2798T>G