Canonical Allele Identifier: PA2825291467
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1348894
ClinVar RCV Id: RCV002035076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys300Ser
CA394983876
NM_001008389.3:c.899G>C
CA394983878
NM_001008389.3:c.898T>A