Allele Registry

Canonical Allele Identifier: PA102888

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000487445

RCV000763619

RCV003139687

ClinVar Variation:

424619

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Ala524Val	CA5056466 NM_005476.7:c.1571C>T