Canonical Allele Identifier: PA2826327109
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 325731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Val490Met
CA8813854
NM_001243342.2:c.1468G>A