Canonical Allele Identifier: PA645425073
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 260958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Pro751Thr
CA8814156
NM_017950.4:c.2251C>A