Canonical Allele Identifier: PA2828750250
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 39418
ClinVar RCV Id: RCV002251328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Cys217Gly
CA261112
NM_001378235.1:c.649T>G