Canonical Allele Identifier: PA2741849900
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2908315
ClinVar RCV Id: RCV003729717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Ser271Thr
CA7939415
NM_001278614.2:c.812G>C