Canonical Allele Identifier: PA2828549993
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 41233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Asp176Val
CA344238
NM_001374797.1:c.527A>T