Canonical Allele Identifier: PA2825291439
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2202214
ClinVar RCV Id: RCV002664028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Arg245His
CA7939413
NM_001008389.3:c.734G>A