Canonical Allele Identifier: PA2828750092
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 318284
ClinVar RCV Id: RCV002520990 RCV002251351 RCV004021646
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365163.1:p.Thr628Asn
CA7939034
NM_001378234.1:c.1883C>A