Canonical Allele Identifier: PA2828749552
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251323
ClinVar Variation:
12260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Asn128Ser
CA256248
NM_001378233.1:c.383A>G