Canonical Allele Identifier: PA202327
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 196363
ClinVar RCV Id: RCV000177175 RCV000968727 RCV002251334 RCV004539648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Leu180Val
CA202326
NM_003361.4:c.538C>G