Canonical Allele Identifier: PA916010511
Gene: UMOD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys250Arg
CA256240
NM_001278614.2:c.748T>C