Canonical Allele Identifier: PA2828749561
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12255
ClinVar RCV Id: RCV002251318 RCV002513003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Cys148Tyr
CA256238
NM_001378233.1:c.443G>A