Canonical Allele Identifier: PA2828749871
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12259
ClinVar RCV Id: RCV002251322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365163.1:p.Cys126Arg
CA256246
NM_001378234.1:c.376T>C