ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828750092
Gene: UMOD
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV002251351
RCV002520990
RCV004021646
ClinVar Variation:
318284
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001365163.1:p.Thr628Asn
CA7939034
NM_001378234.1:c.1883C>A