Canonical Allele Identifier: PA2826157798
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6035
ClinVar RCV Id: RCV000006406 RCV000254883 RCV000763617 RCV004525844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Ala557Val
CA253717
NM_001190383.3:c.1670C>T