Allele Registry

Canonical Allele Identifier: PA915965395

Gene: GGCX HGNC NCBI

ClinVar Variation Id: 789561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000812.2:p.Thr527Ile	CA1741785 NM_000821.7:c.1580C>T