Canonical Allele Identifier: PA2828750449
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 94129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Cys106Phe
CA221976
NM_001378237.1:c.317G>T