Canonical Allele Identifier: PA216155
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 64444
ClinVar RCV Id: RCV000054631 RCV002496729
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Arg588Gln
CA216153
NM_003361.4:c.1763G>A