Allele Registry

Canonical Allele Identifier: PA645386508

Gene: GGCX HGNC NCBI

ClinVar RCV:

RCV000357323

RCV001723929

ClinVar Variation:

337268

HGVS (amino-acid)	Matching Registered Transcripts
NP_000812.2:p.Arg325Gln	CA1741955 NM_000821.7:c.974G>A