Allele Registry

Canonical Allele Identifier: PA916010508

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251328

ClinVar Variation:

39418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Cys250Gly	CA261112 NM_001278614.2:c.748T>G