Canonical Allele Identifier: PA2828750558
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2098927
ClinVar RCV Id: RCV003021466
ClinVar Variation Id: 2630381
ClinVar RCV Id: RCV004527878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Cys282Ser
CA394984102
NM_001378237.1:c.845G>C
CA394984110
NM_001378237.1:c.844T>A