Canonical Allele Identifier: PA102973
Gene: GNE HGNC NCBI
ClinVar RCV:
RCV000006394
ClinVar Variation:
6023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Arg263Leu
CA340505
NM_005476.7:c.788G>T