Canonical Allele Identifier: PA916010546
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 64444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Arg621Gln
CA216153
NM_001278614.2:c.1862G>A