Allele Registry

Canonical Allele Identifier: PA2580170783

Gene: GGCT HGNC NCBI

ClinVar RCV:

RCV004173864

ClinVar Variation:

2337128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186746.1:p.Asp73Asn	CA367120805 NM_001199817.2:c.217G>A