Canonical Allele Identifier: PA2828455800
Gene: UNC80 HGNC NCBI

Linked Data

ClinVar Variation Id: 268207
ClinVar RCV Id: RCV000258922 RCV000963427 RCV001252621 RCV002274004 RCV002518797 RCV003987484 RCV004535244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358915.1:p.Gln602His
CA2082971
NM_001371986.1:c.1806G>C
CA350135716
NM_001371986.1:c.1806G>T