Allele Registry

Canonical Allele Identifier: PA916010492

Gene: UMOD HGNC NCBI

ClinVar Allele:

27298

ClinVar RCV:

RCV002251322

ClinVar Variation:

12259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Cys159Arg	CA256246 NM_001278614.2:c.475T>C