Allele Registry

Canonical Allele Identifier: PA112952

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251328

ClinVar Variation:

39418

HGVS (amino-acid)	Matching Registered Transcripts
NP_001008390.1:p.Cys217Gly	CA261112 NM_001008389.3:c.649T>G