Canonical Allele Identifier: PA2828749580
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 196363
ClinVar RCV Id: RCV000177175 RCV000968727 RCV002251334 RCV004539648
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Leu180Val
CA202326
NM_001378233.1:c.538C>G