Canonical Allele Identifier: PA2829447311
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 3024345
ClinVar RCV Id: RCV003883389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Trp230Arg
CA394985097
NM_003361.4:c.688T>C
CA394985098
NM_003361.4:c.688T>A