Canonical Allele Identifier: PA2826327152
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 215523
ClinVar RCV Id: RCV000195666 RCV000610187 RCV001125861 RCV001657985 RCV003907743
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Thr558Arg
CA335826
NM_001243342.2:c.1673C>G