Canonical Allele Identifier: PA2825291579
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 318284
ClinVar RCV Id: RCV002520990 RCV002251351 RCV004021646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Thr581Asn
CA7939034
NM_001008389.3:c.1742C>A