Canonical Allele Identifier: PA2825291355
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 242346
ClinVar RCV Id: RCV001328178 RCV002251339 RCV002466478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Val93_Gly97delinsAlaAlaSerCys
CA10583988
NM_001008389.3:c.278_289delinsCCGCCTCCT