Canonical Allele Identifier: PA2741849902
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2633167
ClinVar RCV Id: RCV004528774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Gly286Ser
CA394984682
NM_001278614.2:c.856G>A