Canonical Allele Identifier: PA2826608131
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 3066261
ClinVar RCV Id: RCV003991265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys289Ser
CA394984597
NM_001278614.2:c.866G>C
CA394984613
NM_001278614.2:c.865T>A