Canonical Allele Identifier: PA2828750538
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_001365166.1:p.Cys248Ser
CA264233
NM_001378237.1:c.743G>C
CA394984812
NM_001378237.1:c.742T>A