Allele Registry

Canonical Allele Identifier: PA2825291457

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV001566754

RCV002251327

ClinVar Variation:

12264

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008390.1:p.Val273Phe	CA256256 NM_001008389.3:c.817G>T