Canonical Allele Identifier: PA2741849899
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2698818
ClinVar RCV Id: RCV003544325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Pro269Thr
CA394985031
NM_001278614.2:c.805C>A