Canonical Allele Identifier: PA658817662
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 505068
ClinVar RCV Id: RCV000611614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Glu28Gly
CA401345361
NM_017950.4:c.83A>G