Canonical Allele Identifier: PA2828551150
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1462382
ClinVar RCV Id: RCV001954242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361727.1:p.Met139Ile
CA373418004
NM_001374798.1:c.417G>T
CA373418005
NM_001374798.1:c.417G>C
CA373418006
NM_001374798.1:c.417G>A