Allele Registry

Canonical Allele Identifier: PA916010514

Gene: UMOD HGNC NCBI

ClinVar Variation Id: 287876

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Cys281Trp	CA10605900 NM_001278614.2:c.843C>G