Canonical Allele Identifier: PA2825291437
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2124130
ClinVar RCV Id: RCV003057006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Ile242_Arg245del
CA2580090849
NM_001008389.3:c.725_736del