Canonical Allele Identifier: PA2828749980
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1953992
ClinVar RCV Id: RCV002714921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365163.1:p.His314Gln
CA394983718
NM_001378234.1:c.942C>A
CA394983719
NM_001378234.1:c.942C>G