Canonical Allele Identifier: PA658676157
Gene: UNC93B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 470494
ClinVar RCV Id: RCV000545744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112192.2:p.Pro575Gln
CA645582053
NM_030930.4:c.1724_1725delinsAG