Canonical Allele Identifier: PA2830410951
Gene: UNC80 HGNC NCBI

Linked Data

ClinVar Variation Id: 222010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_872393.3:p.Pro1695Ser
CA357888
NM_182587.4:c.5083C>T