Canonical Allele Identifier: PA261113
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251328
ClinVar Variation:
39418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Cys217Gly
CA261112
NM_003361.4:c.649T>G