Canonical Allele Identifier: PA916010493
Gene: UMOD HGNC NCBI
ClinVar RCV:
RCV002251323
ClinVar Variation:
12260
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Asn161Ser
CA256248
NM_001278614.2:c.482A>G