Allele Registry

Canonical Allele Identifier: PA2828749190

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251321

ClinVar Variation:

12258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365161.1:p.Cys77Tyr	CA256244 NM_001378232.1:c.230G>A