Canonical Allele Identifier: PA2828455653
Gene: UNC80 HGNC NCBI

Linked Data

ClinVar Variation Id: 1031498
ClinVar RCV Id: RCV001358347 RCV001333339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358915.1:p.Leu438Pro
CA2082921
NM_001371986.1:c.1313T>C