Canonical Allele Identifier: PA2828749311
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 988207
ClinVar RCV Id: RCV001328228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Cys256Trp
CA394984578
NM_001378232.1:c.768C>G