Canonical Allele Identifier: PA2825291441
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 64644
ClinVar RCV Id: RCV002251329
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008390.1:p.Cys248Ser
CA264233
NM_001008389.3:c.743G>C
CA394984812
NM_001008389.3:c.742T>A