Allele Registry

Canonical Allele Identifier: PA2826344592

Gene: GMNN HGNC NCBI

ClinVar RCV:

RCV000202432

RCV000208587

ClinVar Variation:

204001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001238919.1:p.Lys17Arg	CA250416 NM_001251990.2:c.50A>G