Canonical Allele Identifier: PA2828750279
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1312493
ClinVar RCV Id: RCV002251420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Cys267Phe
CA394984370
NM_001378235.1:c.800G>T