Canonical Allele Identifier: PA2829447327
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 988207
ClinVar RCV Id: RCV001328228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Cys256Trp
CA394984578
NM_003361.4:c.768C>G