Canonical Allele Identifier: PA2828750526
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 3024345
ClinVar RCV Id: RCV003883389
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Trp230Arg
CA394985097
NM_001378237.1:c.688T>C
CA394985098
NM_001378237.1:c.688T>A