Allele Registry

Canonical Allele Identifier: PA2828749662

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV002251372

ClinVar Variation:

441279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365162.1:p.Gln316Pro	CA394983705 NM_001378233.1:c.947A>C