Canonical Allele Identifier: PA2828749647
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 988177
ClinVar RCV Id: RCV001328181 RCV002541644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Ala285Glu
CA394984068
NM_001378233.1:c.854C>A