Canonical Allele Identifier: PA113065
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 521547
ClinVar RCV Id: RCV000624817 RCV001268265 RCV002499013 RCV004527688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Pro236Leu
CA394985022
NM_001008389.3:c.707C>T