Allele Registry

Canonical Allele Identifier: PA2828749821

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV001245586

RCV002251364

RCV004537795

ClinVar Variation:

318297

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365163.1:p.Thr62Pro	CA7939482 NM_001378234.1:c.184A>C