Canonical Allele Identifier: PA2829447342
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 988177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Ala285Glu
CA394984068
NM_003361.4:c.854C>A