Canonical Allele Identifier: PA112974
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 287876
ClinVar RCV Id: RCV000406147 RCV002251342 RCV004535399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys248Trp
CA10605900
NM_001008389.3:c.744C>G