Canonical Allele Identifier: PA658676154
Gene: UNC93B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 470492
ClinVar RCV Id: RCV000557212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112192.2:p.Pro532Thr
CA6145355
NM_030930.4:c.1594C>A