Canonical Allele Identifier: PA2828750507
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251369
ClinVar Variation:
397522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Asp196Gly
CA16609397
NM_001378237.1:c.587A>G