Allele Registry

Canonical Allele Identifier: PA2828749275

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251369

ClinVar Variation:

397522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365161.1:p.Asp196Gly	CA16609397 NM_001378232.1:c.587A>G