Canonical Allele Identifier: PA2826327200
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 215897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Asp673Asn
CA336041
NM_001243342.2:c.2017G>A