Canonical Allele Identifier: PA112858
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_001008390.1:p.Asn128Ser
CA256248
NM_001008389.3:c.383A>G