Allele Registry

Canonical Allele Identifier: PA2825838046

Gene: GGCX HGNC NCBI

ClinVar RCV:

RCV000017579

ClinVar Variation:

16195

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135741.1:p.Trp444Ser	CA126263 NM_001142269.2:c.1331G>C