Canonical Allele Identifier: PA2830080860
Gene: UNC80 HGNC NCBI

Linked Data

ClinVar Variation Id: 1031498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115893.1:p.Leu438Pro
CA2082921
NM_032504.2:c.1313T>C