Canonical Allele Identifier: PA2828749774
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 64444
ClinVar RCV Id: RCV000054631 RCV002496729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Arg588Gln
CA216153
NM_001378233.1:c.1763G>A