Canonical Allele Identifier: PA2828750529
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2698818
ClinVar RCV Id: RCV003544325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Pro236Thr
CA394985031
NM_001378237.1:c.706C>A