Canonical Allele Identifier: PA2742023843
Gene: UBN2 HGNC NCBI
ClinVar RCV:
RCV004301777
ClinVar Variation:
2531428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775840.3:p.Ile383Thr
CA369406904
NM_173569.4:c.1148T>C