Allele Registry

Canonical Allele Identifier: PA2825291417

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251369

ClinVar Variation:

397522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008390.1:p.Asp196Gly	CA16609397 NM_001008389.3:c.587A>G