Canonical Allele Identifier: PA916010540
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251371
ClinVar Variation:
437927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Gly521Asp
CA394982385
NM_001278614.2:c.1562G>A