Canonical Allele Identifier: PA916010538
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 198492
ClinVar RCV Id: RCV000179856 RCV002251335 RCV004539688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Thr502Met
CA247170
NM_001278614.2:c.1505C>T