Canonical Allele Identifier: PA2829447335
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 886536
ClinVar RCV Id: RCV002251396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Gly270Ser
CA7939401
NM_003361.4:c.808G>A