Canonical Allele Identifier: PA112980
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251324
ClinVar Variation:
12261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys255Tyr
CA256250
NM_001008389.3:c.764G>A