Canonical Allele Identifier: PA916010488
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 94129
ClinVar RCV Id: RCV000681797 RCV002251330 RCV004528290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys139Phe
CA221976
NM_001278614.2:c.416G>T