Allele Registry

Canonical Allele Identifier: PA113039

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251320

RCV004528105

ClinVar Variation:

12257

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008390.1:p.Gly103Cys	CA256242 NM_001008389.3:c.307G>T