Allele Registry

Canonical Allele Identifier: PA214958

Gene: GGCX HGNC NCBI

ClinVar RCV:

RCV000017590

RCV001824572

RCV001851893

ClinVar Variation:

16206

HGVS (amino-acid)	Matching Registered Transcripts
NP_000812.2:p.Val255Met	CA214957 NM_000821.7:c.763G>A