Allele Registry

Canonical Allele Identifier: PA2830021619

Gene: GGCT HGNC NCBI

ClinVar RCV:

RCV004173864

ClinVar Variation:

2337128

HGVS (amino-acid)	Matching Registered Transcripts
NP_076956.1:p.Asp167Asn	CA367120805 NM_024051.4:c.499G>A