Allele Registry

Canonical Allele Identifier: PA916010513

Gene: UMOD HGNC NCBI

ClinVar Allele:

75598

ClinVar RCV:

RCV002251329

ClinVar Variation:

64644

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Cys281Ser	CA264233 NM_001278614.2:c.842G>C CA394984812 NM_001278614.2:c.841T>A