Canonical Allele Identifier: PA658655156
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 446167
ClinVar RCV Id: RCV002251373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Cys317Gly
CA394983698
NM_003361.4:c.949T>G