Canonical Allele Identifier: PA113028
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12258
ClinVar RCV Id: RCV002251321
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys77Tyr
CA256244
NM_001008389.3:c.230G>A