Canonical Allele Identifier: PA2825291331
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 318297
ClinVar RCV Id: RCV001245586 RCV002251364 RCV004537795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Thr62Pro
CA7939482
NM_001008389.3:c.184A>C