Canonical Allele Identifier: PA2573194105
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1348894
ClinVar RCV Id: RCV002035076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Cys333Ser
CA394983876
NM_001278614.2:c.998G>C
CA394983878
NM_001278614.2:c.997T>A