Canonical Allele Identifier: PA2830362602
Gene: UBN2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775840.3:p.Lys282Thr
CA4508750
NM_173569.4:c.845A>C