Allele Registry

Canonical Allele Identifier: PA097656

Gene: GCM2 HGNC NCBI

ClinVar RCV:

RCV000006465

RCV002496283

ClinVar Variation:

6092

HGVS (amino-acid)	Matching Registered Transcripts
NP_004743.1:p.Gly63Ser	CA117937 NM_004752.4:c.187G>A