Canonical Allele Identifier: PA2825291438
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2627442
ClinVar RCV Id: RCV003388705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Ile242Asn
CA394984905
NM_001008389.3:c.725T>A