Canonical Allele Identifier: PA174597
Gene: URB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161685
ClinVar RCV Id: RCV000149221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055592.2:p.Gln458Glu
CA174596
NM_014777.2:c.1372C>G