Canonical Allele Identifier: PA112943
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12256
ClinVar RCV Id: RCV002251319
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys217Arg
CA256240
NM_001008389.3:c.649T>C