Canonical Allele Identifier: PA103155
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 464102
ClinVar RCV Id: RCV000532348 RCV001834779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Pro27Ser
CA373421897
NM_005476.7:c.79C>T