Canonical Allele Identifier: PA2829447321
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2124130
ClinVar RCV Id: RCV003057006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Ile242_Arg245del
CA2580090849
NM_003361.4:c.725_736del