Canonical Allele Identifier: PA916010540
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 437927
ClinVar RCV Id: RCV002251371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Gly521Asp
CA394982385
NM_001278614.2:c.1562G>A