Canonical Allele Identifier: PA112904
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_001008390.1:p.Cys148Tyr
CA256238
NM_001008389.3:c.443G>A