Canonical Allele Identifier: PA112952
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 39418
ClinVar RCV Id: RCV002251328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys217Gly
CA261112
NM_001008389.3:c.649T>G