Canonical Allele Identifier: PA2829447320
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 2627442
ClinVar RCV Id: RCV003388705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Ile242Asn
CA394984905
NM_003361.4:c.725T>A