Canonical Allele Identifier: PA2828550053
Gene: GNE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Arg212Leu
CA340505
NM_001374797.1:c.635G>T