Allele Registry

Canonical Allele Identifier: PA2580428016

Gene: RRAGD HGNC NCBI

ClinVar RCV:

RCV002940733

ClinVar Variation:

2334036

HGVS (amino-acid)	Matching Registered Transcripts
NP_067067.1:p.Asp36Gly	CA3920985 NM_021244.4:c.107A>G