Canonical Allele Identifier: PA2829447332
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1312493
ClinVar RCV Id: RCV002251420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Cys267Phe
CA394984370
NM_003361.4:c.800G>T