Allele Registry

Canonical Allele Identifier: PA916010521

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251325

ClinVar Variation:

12262

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Cys333Gly	CA256252 NM_001278614.2:c.997T>G