Allele Registry

Canonical Allele Identifier: PA916010500

Gene: UMOD HGNC NCBI

ClinVar RCV:

RCV000482915

RCV002272254

ClinVar Variation:

423637

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265543.1:p.Tyr216Cys	CA16620080 NM_001278614.2:c.647A>G