Canonical Allele Identifier: PA916010491
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 488632
ClinVar RCV Id: RCV002251374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys153Gly
CA394986277
NM_001278614.2:c.457T>G