Allele Registry

Canonical Allele Identifier: PA2825838030

Gene: GGCX HGNC NCBI

ClinVar RCV:

RCV000017581

RCV003556035

ClinVar Variation:

16197

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135741.1:p.Arg428Pro	CA126264 NM_001142269.2:c.1283G>C