Canonical Allele Identifier: PA916010542
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 253010
ClinVar RCV Id: RCV001233689 RCV002251340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265543.1:p.Asp593Glu
CA7939065
NM_001278614.2:c.1779C>G
CA394980986
NM_001278614.2:c.1779C>A