Canonical Allele Identifier: PA645459293
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 253010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Asp560Glu
CA7939065
NM_003361.4:c.1680C>G
CA394980986
NM_003361.4:c.1680C>A