Canonical Allele Identifier: PA2828749322
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12264
ClinVar RCV Id: RCV001566754 RCV002251327
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Val273Phe
CA256256
NM_001378232.1:c.817G>T