Canonical Allele Identifier: PA2828750464
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 12260
ClinVar RCV Id: RCV002251323
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365166.1:p.Asn128Ser
CA256248
NM_001378237.1:c.383A>G