Allele Registry

Canonical Allele Identifier: PA916010519

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV001566754

RCV002251327

ClinVar Variation:

12264

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Val306Phe	CA256256 NM_001278614.2:c.916G>T