Canonical Allele Identifier: PA2826327237
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 260958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Pro751Thr
CA8814156
NM_001243342.2:c.2251C>A