Canonical Allele Identifier: PA2828750462
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12259
ClinVar RCV Id: RCV002251322
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Cys126Arg
CA256246
NM_001378237.1:c.376T>C