Canonical Allele Identifier: PA916028779
Gene: UNC79 HGNC NCBI

Linked Data

ClinVar Variation Id: 161738
ClinVar RCV Id: RCV000149274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333147.1:p.Thr1443Met
CA174696
NM_001346218.2:c.4328C>T