Canonical Allele Identifier: PA2828749535
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Gly103Cys
CA256242
NM_001378233.1:c.307G>T