Canonical Allele Identifier: PA916010503
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_001265543.1:p.Asp229Gly
CA16609397
NM_001278614.2:c.686A>G