Canonical Allele Identifier: PA2825291448
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 562394
ClinVar RCV Id: RCV000681859 RCV002251376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Trp258Cys
CA394984544
NM_001008389.3:c.774G>T
CA394984546
NM_001008389.3:c.774G>C