Canonical Allele Identifier: PA916010513
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_001265543.1:p.Cys281Ser
CA264233
NM_001278614.2:c.842G>C
CA394984812
NM_001278614.2:c.841T>A