Canonical Allele Identifier: PA357889
Gene: UNC80 HGNC NCBI

Linked Data

ClinVar Variation Id: 222010
ClinVar RCV Id: RCV000207456 RCV001753625
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115893.1:p.Pro1700Ser
CA357888
NM_032504.2:c.5098C>T