Allele Registry

Canonical Allele Identifier: PA916010496

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251318

RCV002513003

ClinVar Variation:

12255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Cys181Tyr	CA256238 NM_001278614.2:c.542G>A