Canonical Allele Identifier: PA2828750559
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 988177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Ala285Glu
CA394984068
NM_001378237.1:c.854C>A