Canonical Allele Identifier: PA645424857
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 325730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Ala487Thr
CA8813850
NM_017950.4:c.1459G>A