Canonical Allele Identifier: PA916010496
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12255
ClinVar RCV Id: RCV002251318 RCV002513003
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys181Tyr
CA256238
NM_001278614.2:c.542G>A