Canonical Allele Identifier: PA2828749654
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12262
ClinVar RCV Id: RCV002251325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Cys300Gly
CA256252
NM_001378233.1:c.898T>G