Allele Registry

Canonical Allele Identifier: PA645386561

Gene: GGCX HGNC NCBI

ClinVar Variation Id: 337260

HGVS (amino-acid)	Matching Registered Transcripts
NP_000812.2:p.Pro636Thr	CA1741686 NM_000821.7:c.1906C>A