Canonical Allele Identifier: PA2828550641
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Val521Leu
CA274932
NM_001374797.1:c.1561G>C
CA373425687
NM_001374797.1:c.1561G>T