Canonical Allele Identifier: PA645509707
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 437927
ClinVar RCV Id: RCV002251371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Gly488Asp
CA394982385
NM_003361.4:c.1463G>A