Canonical Allele Identifier: PA256245
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12258
ClinVar RCV Id: RCV002251321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Cys77Tyr
CA256244
NM_003361.4:c.230G>A