Canonical Allele Identifier: PA2828551249
Gene: GNE HGNC NCBI
ClinVar Allele:
21062
ClinVar RCV:
RCV000006394
ClinVar Variation:
6023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361727.1:p.Arg204Leu
CA340505
NM_001374798.1:c.611G>T