Canonical Allele Identifier: PA2825291444
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2633167
ClinVar RCV Id: RCV004528774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Gly253Ser
CA394984682
NM_001008389.3:c.757G>A