Canonical Allele Identifier: PA112943
Gene: UMOD HGNC NCBI
ClinVar Allele:
27295
ClinVar RCV:
RCV002251319
ClinVar Variation:
12256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys217Arg
CA256240
NM_001008389.3:c.649T>C