Canonical Allele Identifier: PA2828750306
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251373
ClinVar Variation:
446167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Cys317Gly
CA394983698
NM_001378235.1:c.949T>G