Canonical Allele Identifier: PA2828749299
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_001365161.1:p.Ile242_Arg245del
CA2580090849
NM_001378232.1:c.725_736del