Canonical Allele Identifier: PA2828749450
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 318284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Thr581Asn
CA7939034
NM_001378232.1:c.1742C>A