Canonical Allele Identifier: PA916010523
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12263
ClinVar RCV Id: RCV002251326
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys348Arg
CA256254
NM_001278614.2:c.1042T>C