Canonical Allele Identifier: PA2828749190
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12258
ClinVar RCV Id: RCV002251321
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Cys77Tyr
CA256244
NM_001378232.1:c.230G>A