Canonical Allele Identifier: PA2828749297
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2698818
ClinVar RCV Id: RCV003544325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Pro236Thr
CA394985031
NM_001378232.1:c.706C>A