Allele Registry

Canonical Allele Identifier: PA261113

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251328

ClinVar Variation:

39418

HGVS (amino-acid)	Matching Registered Transcripts
NP_003352.2:p.Cys217Gly	CA261112 NM_003361.4:c.649T>G