Canonical Allele Identifier: PA2826608092
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12258
ClinVar RCV Id: RCV002251321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys110Tyr
CA256244
NM_001278614.2:c.329G>A