Allele Registry

Canonical Allele Identifier: PA658806924

Gene: CCDC39 HGNC NCBI

ClinVar RCV:

RCV000629636

RCV003640930

ClinVar Variation:

525559

HGVS (amino-acid)	Matching Registered Transcripts
NP_852091.1:p.Gln91Arg	CA2716208 NM_181426.2:c.272A>G