Canonical Allele Identifier: PA2573072572
Gene: UNC80 HGNC NCBI

Linked Data

ClinVar Variation Id: 222010
ClinVar RCV Id: RCV000207456 RCV001753625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358915.1:p.Pro1766Ser
CA357888
NM_001371986.1:c.5296C>T