Canonical Allele Identifier: PA2828750537
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1012182
ClinVar RCV Id: RCV002251409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Cys248Arg
CA394984811
NM_001378237.1:c.742T>C