Canonical Allele Identifier: PA2828750412
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 318297
ClinVar RCV Id: RCV001245586 RCV002251364 RCV004537795
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Thr62Pro
CA7939482
NM_001378237.1:c.184A>C