Canonical Allele Identifier: PA2828750225
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 423637
ClinVar RCV Id: RCV000482915 RCV002272254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Tyr183Cys
CA16620080
NM_001378235.1:c.548A>G