Canonical Allele Identifier: PA2828749303
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251329
ClinVar Variation:
64644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Cys248Ser
CA264233
NM_001378232.1:c.743G>C
CA394984812
NM_001378232.1:c.742T>A