Canonical Allele Identifier: PA2826327105
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 325730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Ala487Thr
CA8813850
NM_001243342.2:c.1459G>A