Canonical Allele Identifier: PA2828455283
Gene: UNC80 HGNC NCBI

Linked Data

ClinVar Variation Id: 1441474
ClinVar RCV Id: RCV001950646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358915.1:p.His84Tyr
CA2082697
NM_001371986.1:c.250C>T