Canonical Allele Identifier: PA2828750205
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Cys148Tyr
CA256238
NM_001378235.1:c.443G>A