Canonical Allele Identifier: PA2825291538
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 198492
ClinVar RCV Id: RCV000179856 RCV002251335 RCV004539688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Thr469Met
CA247170
NM_001008389.3:c.1406C>T