Canonical Allele Identifier: PA2741849898
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 3024345
ClinVar RCV Id: RCV003883389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Trp263Arg
CA394985097
NM_001278614.2:c.787T>C
CA394985098
NM_001278614.2:c.787T>A