Allele Registry

Canonical Allele Identifier: PA102905

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV004576690

ClinVar Variation:

3241709

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Ala630Thr	CA373425049 NM_005476.7:c.1888G>A