Canonical Allele Identifier: PA2828750507
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 397522
ClinVar RCV Id: RCV002251369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Asp196Gly
CA16609397
NM_001378237.1:c.587A>G