Canonical Allele Identifier: PA2828750188
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 488632
ClinVar RCV Id: RCV002251374
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Cys120Gly
CA394986277
NM_001378235.1:c.358T>G